Albumin fusion proteins

ABSTRACT

The present invention encompasses albumin fusion proteins. Nucleic acid molecules encoding the albumin fusion proteins of the invention are also encompassed by the invention, as are vectors containing these nucleic acids, host cells transformed with these nucleic acids vectors, and methods of making the albumin fusion proteins of the invention and using these nucleic acids, vectors, and/or host cells. Additionally the present invention encompasses pharmaceutical compositions comprising albumin fusion proteins and methods of treating, preventing, or ameliorating diseases, disorders or conditions using albumin fusion proteins of the invention.

BACKGROUND OF THE INVENTION

The invention relates generally to Therapeutic proteins (including, butnot limited to, at least one polypeptide, antibody, peptide, or fragmentand variant thereof) fused to albumin or fragments or variants ofalbumin. The invention encompasses polynucleotides encoding therapeuticalbumin fusion proteins, therapeutic albumin fusion proteins,compositions, pharmaceutical compositions, formulations and kits. Hostcells transformed with the polynucleotides encoding therapeutic albuminfusion proteins are also encompassed by the invention, as are methods ofmaking the albumin fusion proteins of the invention using thesepolynucleotides, and/or host cells.

Human serum albumin (HSA, or HA), a protein of 585 amino acids in itsmature form (as shown in FIG. 1 (SEQ ID NO:1038)), is responsible for asignificant proportion of the osmotic pressure of serum and alsofunctions as a carrier of endogenous and exogenous ligands. At present,HA for clinical use is produced by extraction from human blood. Theproduction of recombinant HA (rHA) in microorganisms has been disclosedin EP 330 451 and EP 361 991.

Therapeutic proteins in their native state or when recombinantlyproduced, such as interferons and growth hormones, are typically labilemolecules exhibiting short shelf-lives, particularly when formulated inaqueous solutions. The instability in these molecules when formulatedfor administration dictates that many of the molecules must belyophilized and refrigerated at all times during storage, therebyrendering the molecules difficult to transport and/or store. Storageproblems are particularly acute when pharmaceutical formulations must bestored and dispensed outside of the hospital environment.

Few practical solutions to the storage problems of labile proteinmolecules have been proposed. Accordingly, there is a need forstabilized, long lasting formulations of proteinaceous therapeuticmolecules that are easily dispensed, preferably with a simpleformulation requiring minimal post-storage manipulation.

SUMMARY OF THE INVENTION

The present invention encompasses albumin fusion proteins comprising aTherapeutic protein (e.g., a polypeptide, antibody, or peptide, orfragment or variant thereof) fused to albumin or a fragment (portion) orvariant of albumin. The present invention also encompassespolynucleotides comprising, or alternatively consisting of, nucleic acidmolecules encoding a Therapeutic protein (e.g., a polypeptide, antibody,or peptide, or fragment or variant thereof) fused to albumin or afragment (portion) or variant of albumin. The present invention alsoencompasses polynucleotides, comprising, or alternatively consisting of,nucleic acid molecules encoding proteins comprising a Therapeuticprotein (e.g., a polypeptide, antibody, or peptide, or fragment orvariant thereof) fused to albumin or a fragment (portion) or variant ofalbumin, that is sufficient to prolong the shelf life of the Therapeuticprotein, and/or stabilize the Therapeutic protein and/or its activity insolution (or in a pharmaceutical composition) in vitro and/or in vivo.Albumin fusion proteins encoded by a polynucleotide of the invention arealso encompassed by the invention, as are host cells transformed withpolynucleotides of the invention, and methods of making the albuminfusion proteins of the invention and using these polynucleotides of theinvention, and/or host cells.

In a preferred aspect of the invention, albumin fusion proteins include,but are not limited to, those encoded by the polynucleotides describedin Table 2.

The invention also encompasses pharmaceutical formulations comprising analbumin fusion protein of the invention and a pharmaceuticallyacceptable diluent or carrier. Such formulations may be in a kit orcontainer. Such kit or container may be packaged with instructionspertaining to the extended shelf life of the Therapeutic protein. Suchformulations may be used in methods of treating, preventing,ameliorating or diagnosing a disease or disease symptom in a patient,preferably a mammal, most preferably a human, comprising the step ofadministering the pharmaceutical formulation to the patient.

In other embodiments, the present invention encompasses methods ofpreventing, treating, or ameliorating a disease or disorder. Inpreferred embodiments, the present invention encompasses a method oftreating a disease or disorder listed in the “Preferred Indication: Y”column of Table 1 comprising administering to a patient in which suchtreatment, prevention or amelioration is desired an albumin fusionprotein of the invention that comprises a Therapeutic protein or portioncorresponding to a Therapeutic protein (or fragment or variant thereof)disclosed in the “Therapeutic Protein: X” column of Table 1 (in the samerow as the disease or disorder to be treated is listed in the “PreferredIndication: Y” column of Table 1) in an amount effective to treat,prevent or ameliorate the disease or disorder.

In one embodiment, an albumin fusion protein described in Table 1 or 2has extended shelf life.

In a second embodiment, an albumin fusion protein described in Table 1or 2 is more stable than the corresponding unfused Therapeutic moleculedescribed in Table 1.

The present invention further includes transgenic organisms modified tocontain the nucleic acid molecules of the invention (including, but notlimited to, the polynucleotides described in Tables 1 and 2), preferablymodified to express an albumin fusion protein of the invention.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A-D shows the amino acid sequence of the mature form of humanalbumin (SEQ ID NO:1038) and a polynucleotide encoding it (SEQ IDNO:1037).

FIG. 2 shows the restriction map of the pPPC0005 cloning vector ATCCdeposit PTA-3278.

FIG. 3 shows the restriction map of the pSAC35 yeast S. cerevisiaeexpression vector (Sleep et al., BioTechnology 8:42 (1990)).

FIG. 4 shows the effect of various dilutions of EPO albumin fusionproteins encoded by DNA comprised in Construct ID NOS. (hereinafter CID)1966 and 1981 and recombinant human EPO on the proliferation of TF-1cells (see Examples 8 and 9). Cells were washed 3× to remove GM-CSF andplated at 10,000 cells/well for 72 hours in the presence of 3-folddilutions of CID 1966 protein or CID 1981 protein. Concentrations usedwere calculated based on the weight of Epo alone, not HSA plus Epo.Recombinant human Epo (rhEpo) was used as the positive control andserially diluted 3 fold from 100 ng/ml to 0.01 ng/ml. Cells were exposedto 0.5 mCi/well of ³H-thymidine for an additional 18 hours. (□) rhEpo;(▾) HSA-Epo 1981; () Epo-HSA 1966.

FIG. 5 is a dose response analysis and shows the effect of various dosesof recombinant human EPO and EPO albumin fusion proteins encoded by DNAcomprised in CID 1966 and 1981 on the percent change in hematocrit fromday 0 to day 7 (see Examples 8 and 9). 48 eight-week old femaleDBA/2NHsd mice were divided into 12 groups of 4 animals each.Recombinant human Epo (rhEpo) was administered subcutaneously at 0.5,1.5, 4.5 and 12 μs/kg on days 0, 2, 4, and 6. Epo albumin fusionproteins made from constructs CID 1966 and CID 1981 were administeredsubcutaneously at 2, 6, 18, and 54 μs/kg on days 0, 2, 4, and 6. Thehigher doses of the Epo albumin fusion proteins allows a rough equimolarcomparison with recombinant human Epo (note that the weight of thefusions is about 4.35 times the weight of non-glycosylated Epo). On days0 and 7 of the experiment, the animals were bled via a tail vein and thehematocrit was determined by centrifugation. (▪) rhEpo; (◯) CID 1981;(σ) CID 1966.

FIG. 6A shows the effect of various subcutaneous administrations of Epoalbumin fusion proteins encoded by DNA comprised in CID 1966 and 1997,respectively, on the percent change in hematocrit from day 0 to day 8(see Examples 8 and 10). *, p<0.005 compared to rhEpo as determined byMann-Whitney nonparametric analysis (n=6).

FIG. 6B shows the effect of subcutaneous administrations of Epo albuminfusion proteins encoded by DNA comprised in CID 1997 and 1966 on thepercent change in hematocrit from day 0 to day 14 (see Examples 8 and10). *, p<0.005 compared to rhEpo as determined by Mann-Whitneynonparametric analysis (n=6); **, p<0.05 compared to rhEpo as determinedby Mann-Whitney nonparametric analysis (n=6).

FIG. 7 shows the effect of various dilutions albumin fusion proteinsencoded by DNA comprised in CID 1981 and 1997, respectively, on theproliferation of TF-1 cells (see Examples 9 and 10). Cells were washed3× to remove GM-CSF and plated at 10,000 cells/well for 72 hours in thepresence of 3-fold dilutions of Epo albumin fusion proteins encoded byCID 1981 or 1997. Equimolar amounts of rhEpo were used as a positivecontrol (4.35 times less protein added since weight of non-glycosylatedEpo is 20 kd, while Epo albumin fusion proteins are 87 kd). Cells wereexposed to 0.5 μCi/well of ³H-thymidine for an additional 24 hours. (▪)rhEpo Standard; (σ) CID 1981 (CHO); (◯) CID 1997 (NSO).

FIG. 8 shows the effect of various doses of recombinant human EPO(rhEpo) and EPO albumin fusion protein encoded by DNA comprised inconstruct 1997 (CID 1997) on the percent change in hematocrit from day 0to day 8 (see Example 10). (σ)=rhEpo, (□)=CID 1997.

FIG. 9 shows the effect of various dilutions of IL2 albumin fusionproteins encoded by DNA comprised in CID 1812 (see Example 15) on CTLL-2proliferation. 1×10⁴ cells/well were seeded in a 96-well plate in afinal volume of 200 ul of complete medium containing the indicatedamount of IL2 albumin fusion protein (CID 1812). All samples were run intriplicate. The cells were incubated for 40 hours at 37° C., then 20 ulof Alamar Blue was added and cells incubated for 8 hours. Absorbance at530/590 was used as a measure of proliferation. EC50=0.386±0.021.(Δ)=CID 1812.

FIG. 10 shows the effect of IL2 albumin fusion protein encoded by DNAcomprised in CID 1812 on RENCA tumor growth at day 21 (see Example 15).BALB/c mice (n=10) were injected SC (midflank) with 10⁵ RENCA cells. 10days later mice received 2 cycles (Day 10 to Day 14 and Days 17-21) ofdaily (QD) injections of rIL2 (0.9 mg/kg), IL2 albumin fusion protein(CID 1812 protein; 0.6 mg/kg), or PBS (Placebo) or injections everyother day (QOD) of CID 1812 protein (0.6 mg/kg). The tumor volume wasdetermined on Day 21 after RENCA inoculation. The data are presented inscatter analysis (each dot representing single animal). Mean value ofeach group is depicted by horizontal line. *, p=0.0035 between placebocontrol and CID 1812 protein. The number in parentheses indicates numberof mice alive over the total number of mice per group. (◯)=Placebo;()=IL2; (Δ)=CID 1812 protein (QD); (□)=CID 1812 protein (QOD).

FIG. 11 shows the effect of various dilutions of GCSF albumin fusionproteins encoded by DNA comprised in CID 1642 and 1643 on NFS-60 cellproliferation (see Examples 19 and 20). (▪)=CID 1642; (σ)=CID 1643;(◯)=HSA.

FIG. 12 shows the effect of recombinant human GCSF (Neupogen) and GCSFalbumin fusion protein on total white blood cell count (see Example 19).Total WBC (10³ cells/ul) on each day are presented as the groupmean±SEM. GCSF albumin fusion protein was administered sc at either 25or 100 ug/kg every 4 days×4 (Q4D), or at 100 ug/kg every 7 days×2 (Q7D).Data from Days 8 and 9 for GCSF albumin fusion protein 100 ug/kg Q7 arepresented as Days 9 and 10, respectively, to facilitate comparison withother groups. Controls were saline vehicle administered SC every 4days×4 (Vehicle Q4D), or Neupogen administered SC daily×14 (Neupogen 5ug/kg QD). The treatment period is considered Days 1-14, and therecovery period, Days 15-28.

FIG. 13 shows the effect of various dilutions of IFNb albumin fusionproteins encoded by DNA comprised in CID 2011 and 2053 on SEAP activityin the ISRE-SEAP/293F reporter cells (see Example 25). Proteins wereserially diluted from 5e-7 to 1e-14 g/ml in DMEM/10% FBS and used totreat ISRE-SEAP/293F reporter cells. After 24 hours supernatants wereremoved from reporter cells and assayed for SEAP activity. IFNb albuminfusion protein was purified from three stable clones: 293F/#2011,CHO/#2011 and NSO/#2053. Mammalian derived IFNb, Avonex, came fromBiogen and was reported to have a specific activity of 2.0e5 IU/ug.

FIG. 14 illustrates the steady-state levels of insulin mRNA in INS-1(832/13) cells after treatment with GLP-1 or GLP-1 albumin fusionprotein encoded by construct ID 3070 (CID 3070 protein). Both GLP-1 andthe CID 3070 protein stimulate transcription of the insulin gene inINS-1 cells. The first bar (black) represents the untreated cells. Bars2-4 (white) represent cells treated with the indicated concentrations ofGLP-1. Bars 5-7 (gray) represent cells treated with the indicatedconcentrations of CID 3070 protein.

FIG. 15 compares the anti-proliferative activity of IFN albumin fusionprotein encoded by CID 3165 (CID 3165 protein) and recombinant IFNa(rIFNa) on Hs294T melanoma cells. The cells were cultured with varyingconcentrations of either CID 3165 protein or rIFNa and proliferation wasmeasured by BrdU incorporation after 3 days of culture. CID 3165 proteincaused measurable inhibition of cell proliferation at concentrationsabove 10 ng/ml with 50% inhibition achieved at approximately 200 ng/ml.(▪)=CID 3165 protein, (♦)=rIFNa.

FIG. 16 shows the effect of various dilutions of IFNa albumin fusionproteins on SEAP activity in the ISRE-SEAP/293F reporter cells. Onepreparation of IFNa fused upstream of albumin (♦) was tested, as well astwo different preparations of IFNa fused downstream of albumin (σ) and(▪).

FIG. 17 shows the effect of time and dose of IFNa albumin fusion proteinencoded by DNA comprised in construct 2249 (CID 2249 protein) on themRNA level of OAS (p41) in treated monkeys (see Example 31). Per timepoint: first bar=Vehicle control, 2^(nd) bar=30 ug/kg CID 2249 proteinday 1 iv, third bar=30 ug/kg CID 2249 protein day 1 sc, 4^(th) bar=300ug/kg CID 2249 protein day 1 sc, 5^(th) bar=40 ug/kg recombinant IFNaday 1, 3 and 5 sc.

FIG. 18 shows the effect of various dilutions of insulin albumin fusionproteins encoded by DNA comprised in constructs 2250 and 2276 on glucoseuptake in 3T3-L1 adipocytes (see Examples 33 and 35).

FIG. 19 shows the effect of various GCSF albumin fusion proteins,including those encoded by CID #1643 and #2702 (L-171, see Example 114),on NFS cell proliferation. The horizontal dashed line indicates theminimum level of detection.

DETAILED DESCRIPTION Definitions

The following definitions are provided to facilitate understanding ofcertain terms used throughout this specification.

As used herein, “polynucleotide” refers to a nucleic acid moleculehaving a nucleotide sequence encoding a fusion protein comprising, oralternatively consisting of, at least one molecule of albumin (or afragment or variant thereof) joined in frame to at least one Therapeuticprotein X (or fragment or variant thereof); a nucleic acid moleculehaving a nucleotide sequence encoding a fusion protein comprising, oralternatively consisting of, the amino acid sequence of SEQ ID NO:Y (asdescribed in column 6 of Table 2) or a fragment or variant thereof; anucleic acid molecule having a nucleotide sequence comprising oralternatively consisting of the sequence shown in SEQ ID NO:X; a nucleicacid molecule having a nucleotide sequence encoding a fusion proteincomprising, or alternatively consisting of, the amino acid sequence ofSEQ ID NO:Z; a nucleic acid molecule having a nucleotide sequenceencoding an albumin fusion protein of the invention generated asdescribed in Table 2 or in the Examples; a nucleic acid molecule havinga nucleotide sequence encoding a Therapeutic albumin fusion protein ofthe invention, a nucleic acid molecule having a nucleotide sequencecontained in an albumin fusion construct described in Table 2, or anucleic acid molecule having a nucleotide sequence contained in analbumin fusion construct deposited with the ATCC (as described in Table3).

As used herein, “albumin fusion construct” refers to a nucleic acidmolecule comprising, or alternatively consisting of, a polynucleotideencoding at least one molecule of albumin (or a fragment or variantthereof) joined in frame to at least one polynucleotide encoding atleast one molecule of a Therapeutic protein (or fragment or variantthereof); a nucleic acid molecule comprising, or alternativelyconsisting of, a polynucleotide encoding at least one molecule ofalbumin (or a fragment or variant thereof) joined in frame to at leastone polynucleotide encoding at least one molecule of a Therapeuticprotein (or fragment or variant thereof) generated as described in Table2 or in the Examples; or a nucleic acid molecule comprising, oralternatively consisting of, a polynucleotide encoding at least onemolecule of albumin (or a fragment or variant thereof) joined in frameto at least one polynucleotide encoding at least one molecule of aTherapeutic protein (or fragment or variant thereof), furthercomprising, for example, one or more of the following elements: (1) afunctional self-replicating vector (including but not limited to, ashuttle vector, an expression vector, an integration vector, and/or areplication system), (2) a region for initiation of transcription (e.g.,a promoter region, such as for example, a regulatable or induciblepromoter, a constitutive promoter), (3) a region for termination oftranscription, (4) a leader sequence, and (5) a selectable marker. Thepolynucleotide encoding the Therapeutic protein and albumin protein,once part of the albumin fusion construct, may each be referred to as a“portion,” “region” or “moiety” of the albumin fusion construct.

The present invention relates generally to polynucleotides encodingalbumin fusion proteins; albumin fusion proteins; and methods oftreating, preventing, or ameliorating diseases or disorders usingalbumin fusion proteins or polynucleotides encoding albumin fusionproteins. As used herein, “albumin fusion protein” refers to a proteinformed by the fusion of at least one molecule of albumin (or a fragmentor variant thereof) to at least one molecule of a Therapeutic protein(or fragment or variant thereof). An albumin fusion protein of theinvention comprises at least a fragment or variant of a Therapeuticprotein and at least a fragment or variant of human serum albumin, whichare associated with one another by genetic fusion (i.e., the albuminfusion protein is generated by translation of a nucleic acid in which apolynucleotide encoding all or a portion of a Therapeutic protein isjoined in-frame with a polynucleotide encoding all or a portion ofalbumin). The Therapeutic protein and albumin protein, once part of thealbumin fusion protein, may each be referred to as a “portion”, “region”or “moiety” of the albumin fusion protein (e.g., a “Therapeutic proteinportion” or an “albumin protein portion”). In a highly preferredembodiment, an albumin fusion protein of the invention comprises atleast one molecule of a Therapeutic protein X or fragment or variant ofthereof (including, but not limited to a mature form of the Therapeuticprotein X) and at least one molecule of albumin or fragment or variantthereof (including but not limited to a mature form of albumin).

In a further preferred embodiment, an albumin fusion protein of theinvention is processed by a host cell and secreted into the surroundingculture medium. Processing of the nascent albumin fusion protein thatoccurs in the secretory pathways of the host used for expression mayinclude, but is not limited to signal peptide cleavage; formation ofdisulfide bonds; proper folding; addition and processing ofcarbohydrates (such as for example, N- and O-linked glycosylation);specific proteolytic cleavages; and assembly into multimeric proteins.An albumin fusion protein of the invention is preferably in theprocessed form. In a most preferred embodiment, the “processed form ofan albumin fusion protein” refers to an albumin fusion protein productwhich has undergone N-terminal signal peptide cleavage, herein alsoreferred to as a “mature albumin fusion protein”.

In several instances, a representative clone containing an albuminfusion construct of the invention was deposited with the American TypeCulture Collection (herein referred to as “ATCC®”). Furthermore, it ispossible to retrieve a given albumin fusion construct from the depositby techniques known in the art and described elsewhere herein. The ATCC®is located at 10801 University Boulevard, Manassas, Va. 20110-2209, USA.The ATCC® deposits were made pursuant to the terms of the BudapestTreaty on the international recognition of the deposit of microorganismsfor the purposes of patent procedure.

In one embodiment, the invention provides a polynucleotide encoding analbumin fusion protein comprising, or alternatively consisting of, aTherapeutic protein and a serum albumin protein. In a furtherembodiment, the invention provides an albumin fusion protein comprising,or alternatively consisting of, a Therapeutic protein and a serumalbumin protein. In a preferred embodiment, the invention provides analbumin fusion protein comprising, or alternatively consisting of, aTherapeutic protein and a serum albumin protein encoded by apolynucleotide described in Table 2. In a further preferred embodiment,the invention provides a polynucleotide encoding an albumin fusionprotein whose sequence is shown as SEQ ID NO:Y in Table 2. In otherembodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a biologically active and/ortherapeutically active fragment of a Therapeutic protein and a serumalbumin protein. In other embodiments, the invention provides an albuminfusion protein comprising, or alternatively consisting of, abiologically active and/or therapeutically active variant of aTherapeutic protein and a serum albumin protein. In preferredembodiments, the serum albumin protein component of the albumin fusionprotein is the mature portion of serum albumin. The invention furtherencompasses polynucleotides encoding these albumin fusion proteins.

In further embodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a Therapeutic protein, and abiologically active and/or therapeutically active fragment of serumalbumin. In further embodiments, the invention provides an albuminfusion protein comprising, or alternatively consisting of, a Therapeuticprotein and a biologically active and/or therapeutically active variantof serum albumin. In preferred embodiments, the Therapeutic proteinportion of the albumin fusion protein is the mature portion of theTherapeutic protein. In a further preferred embodiment, the Therapeuticprotein portion of the albumin fusion protein is the extracellularsoluble domain of the Therapeutic protein. In an alternative embodiment,the Therapeutic protein portion of the albumin fusion protein is theactive form of the Therapeutic protein. The invention furtherencompasses polynucleotides encoding these albumin fusion proteins.

In further embodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a biologically active and/ortherapeutically active fragment or variant of a Therapeutic protein anda biologically active and/or therapeutically active fragment or variantof serum albumin. In preferred embodiments, the invention provides analbumin fusion protein comprising, or alternatively consisting of, themature portion of a Therapeutic protein and the mature portion of serumalbumin. The invention further encompasses polynucleotides encodingthese albumin fusion proteins.

Therapeutic Proteins

As stated above, a polynucleotide of the invention encodes a proteincomprising or alternatively consisting of, at least a fragment orvariant of a Therapeutic protein and at least a fragment or variant ofhuman serum albumin, which are associated with one another, preferablyby genetic fusion.

An additional embodiment includes a polynucleotide encoding a proteincomprising or alternatively consisting of at least a fragment or variantof a Therapeutic protein and at least a fragment or variant of humanserum albumin, which are linked with one another by chemicalconjugation.

As used herein, “Therapeutic protein” refers to proteins, polypeptides,antibodies, peptides or fragments or variants thereof, having one ormore therapeutic and/or biological activities. Therapeutic proteinsencompassed by the invention include but are not limited to, proteins,polypeptides, peptides, antibodies, and biologics. (The terms peptides,proteins, and polypeptides are used interchangeably herein.) It isspecifically contemplated that the term “Therapeutic protein”encompasses antibodies and fragments and variants thereof. Thus aprotein of the invention may contain at least a fragment or variant of aTherapeutic protein, and/or at least a fragment or variant of anantibody. Additionally, the term “Therapeutic protein” may refer to theendogenous or naturally occurring correlate of a Therapeutic protein.

By a polypeptide displaying a “therapeutic activity” or a protein thatis “therapeutically active” is meant a polypeptide that possesses one ormore known biological and/or therapeutic activities associated with atherapeutic protein such as one or more of the Therapeutic proteinsdescribed herein or otherwise known in the art. As a non-limitingexample, a “Therapeutic protein” is a protein that is useful to treat,prevent or ameliorate a disease, condition or disorder. As anon-limiting example, a “Therapeutic protein” may be one that bindsspecifically to a particular cell type (normal (e.g., lymphocytes) orabnormal e.g., (cancer cells)) and therefore may be used to target acompound (drug, or cytotoxic agent) to that cell type specifically.

For example, a non-exhaustive list of “Therapeutic protein” portionswhich may be comprised by an albumin fusion protein of the inventionincludes, but is not limited to, erythropoietin (EPO), IL-2, G-CSF,Insulin, Calcitonin, Growth Hormone, IFN-alpha, IFN-beta, PTH, TR6(International Publication No. WO 98/30694), BLyS, BLyS single chainantibody, Resistin, Growth hormone releasing factor, VEGF-2, KGF-2,D-SLAM, KDI, and TR2, GLP-1, Extendin 4, and GM-CSF.

Interferon hybrids may also be fused to the amino or carboxy terminus ofalbumin to form an interferon hybrid albumin fusion protein. Interferonhybrid albumin fusion protein may have enhanced, or alternatively,suppressed interferon activity, such as antiviral responses, regulationof cell growth, and modulation of immune response (Lebleu et al., PNASUSA, 73:3107-3111 (1976); Gresser et al., Nature, 251:543-545 (1974);and Johnson, Texas Reports Biol Med, 35:357-369 (1977)). Each interferonhybrid albumin fusion protein can be used to treat, prevent, orameliorate viral infections (e.g., hepatitis (e.g., HCV); or HIV),multiple sclerosis, or cancer.

In one embodiment, the interferon hybrid portion of the interferonhybrid albumin fusion protein comprises an interferon alpha-interferonalpha hybrid (herein referred to as an alpha-alpha hybrid). For example,the alpha-alpha hybrid portion of the interferon hybrid albumin fusionprotein consists, or alternatively comprises, of interferon alpha Afused to interferon alpha D. In a further embodiment, the A/D hybrid isfused at the common BgIII restriction site to interferon alpha D,wherein the N-terminal portion of the A/D hybrid corresponds to aminoacids 1-62 of interferon alpha A and the C-terminal portion correspondsto amino acids 64-166 of interferon alpha D. For example, this A/Dhybrid would comprise the amino acid sequence:

(SEQ ID NO: 1326) CDLPQTHSLGSRRTLMLLAQMRX₁ISLFSCLKDRHDFGFPQEEFGNQFQKAETIPVLHEMIQQIFNLFTTKDSSAAWDEDLLDKFCTELYQQLNDLEACVMQEERVGETPLMNX₂DSILAVKKYFRRITLYLTEKKYSPCAWEVVRA EIMIRSLSLSTNLQERLRRKE,wherein the X₁ is R or K and the X₂ is A or V (see, for example,Construct ID #2875). In an additional embodiment, the A/D hybrid isfused at the common PvuIII restriction site, wherein the N-terminalportion of the A/D hybrid corresponds to amino acids 1-91 of interferonalpha A and the C-terminal portion corresponds to amino acids 93-166 ofinterferon alpha D. For example, this A/D hybrid would comprise theamino acid sequence:

(SEQ ID NO: 1311) CDLPQTHSLGSRRTLMLLAQMRX₁ISLFSCLKDRHDFGFPQEEFGNQFQKAETIPVLHEMIQQIFNLFSTKDSSAAWDETLLDKFYTELYQQLNDLEACVMQEERVGETPLMNX₂DSILAVKKYFRRITLYLTEKKYSPCAWEVVRAEIM IRSLSLSTNLQERLRRKE,wherein the X₁ is R or K and the second X₂ is A or V (see, for example,Construct ID #2872). These hybrids are further described in U.S. Pat.No. 4,414,510, which is hereby incorporated by reference in itsentirety.

In an additional embodiment, the alpha-alpha hybrid portion of theinterferon hybrid albumin fusion protein consists, or alternativelycomprises, of interferon alpha A fused to interferon alpha F. In afurther embodiment, the A/F hybrid is fused at the common PvuIIIrestriction site, wherein the N-terminal portion of the A/F hybridcorresponds to amino acids 1-91 of interferon alpha A and the C-terminalportion corresponds to amino acids 93-166 of interferon alpha F. Forexample, this A/F hybrid would comprise the amino acid sequence:

(SEQ ID NO: 1321) CDLPQTHSLGSRRTLMLLAQMRXISLFSCLKDRHDFGFPQEEFGNQFQKAETIPVLHEMIQQIFNLFSTKDSSAAWDETLLDKFYTELYQQLNDMEACVIQEVGVEETPLMNVDSILAVKKYFQRITLYLTEKKYSPCAWEVVRAEIMRS FSLSKIFQERLRRKE,wherein X is either R or K (see, for example, Construct ID #2874). Thesehybrids are further described in U.S. Pat. No. 4,414,510, which ishereby incorporated by reference in its entirety. In a furtherembodiment, the alpha-alpha hybrid portion of the interferon hybridalbumin fusion protein consists, or alternatively comprises, ofinterferon alpha A fused to interferon alpha B. In an additionalembodiment, the A/B hybrid is fused at the common PvuIII restrictionsite, wherein the N-terminal portion of the A/B hybrid corresponds toamino acids 1-91 of interferon alpha A and the C-terminal portioncorresponds to amino acids 93-166 of interferon alpha B. For example,this A/B hybrid would comprise an amino acid sequence:

(SEQ ID NO: 1316) CDLPQTHSLGSRRTLMLLAQMRX₁ISLFSCLKDRHDFGFPQEEFGNQFQKAETIPVLHEMIQQIFNLFSTKDSSAAWDETLLDKFYTELYQQLNDLEX₂X₃X₄X₅QEVGVIESPLMYEDSILAVRKYFQRITLYLTEKKYSSCAWEVVRAEI MRSFSLSINLQKRLKSKE,wherein the X₁ is R or K and X₂ through X₅ is SCVM or VLCD (see, forexample, Construct ID #2873). These hybrids are further described inU.S. Pat. No. 4,414,510, which is hereby incorporated by reference inits entirety.

In another embodiment, the interferon hybrid portion of the interferonhybrid albumin fusion protein comprises an interferon beta-interferonalpha hybrid (herein referred to as a beta-alpha hybrid). For example,the beta-alpha hybrid portion of the interferon hybrid albumin fusionprotein consists, or alternatively comprises, of interferon beta-1 fusedto interferon alpha D (also referred to as interferon alpha-1). In afurther embodiment, the beta-1/alpha D hybrid is fused wherein theN-terminal portion corresponds to amino acids 1-73 of interferon beta-1and the C-terminal portion corresponds to amino acids 74-167 ofinterferon alpha D. For example, this beta-1/alpha D hybrid wouldcomprise an amino acid sequence:

(SEQ ID NO: 2130) MSYNLLGFLQRSSNFQCQKLLWQLNGRLEYCLKDRMNFDIPEEIKQLQQFQKEDAALTIYEMLQNIFAIFRQDSSAAWDEDLLDKFCTELYQQLNDLEACVMQEERVGETPLMNXDSILAVKKYFRRITLYLTEKKYSPCAWEVVRAEIM RSLSLSTNLQERLRRKE,wherein X is A or V. These hybrids are further described in U.S. Pat.No. 4,758,428, which is hereby incorporated by reference in itsentirety.

In another embodiment, the interferon hybrid portion of the interferonhybrid albumin fusion protein comprises an interferon alpha-interferonbeta hybrid (herein referred to as a alpha-beta hybrid). For example,the alpha-beta hybrid portion of the interferon hybrid albumin fusionprotein consists, or alternatively comprises, of interferon alpha D(also referred to as interferon alpha-1) fused to interferon beta-1. Ina further embodiment, the alpha D/beta-1 hybrid is fused wherein theN-terminal portion corresponds to amino acids 1-73 of interferon alpha Dand the C-terminal portion corresponds to amino acids 74-166 ofinterferon beta-1. For example, this alpha D/beta-1 hybrid would have anamino acid sequence:

(SEQ ID NO: 2131) MCDLPETHSLDNRRTLMLLAQMSRISPSSCLMDRHDFGFPQEEFDGNQFQKAPAISVLHELIQQIFNLFTTKDSSSTGWNETIVENLLANVYHQINHLKTVLEEKLEKEDFTRGKLMSSLHLKRYYGRILHYLKAKEYSHCAWTIVRVEI LRNFYFINRLTGYLRN.

These hybrids are further described in U.S. Pat. No. 4,758,428, which ishereby incorporated by reference in its entirety.

In further embodiments, the interferon hybrid portion of the interferonhybrid albumin fusion proteins may comprise additional combinations ofalpha-alpha interferon hybrids, alpha-beta interferon hybrids, andbeta-alpha interferon hybrids. In additional embodiments, the interferonhybrid portion of the interferon hybrid albumin fusion protein may bemodified to include mutations, substitutions, deletions, or additions tothe amino acid sequence of the interferon hybrid. Such modifications tothe interferon hybrid albumin fusion proteins may be made, for example,to improve levels of production, increase stability, increase ordecrease activity, or confer new biological properties.

The above-described interferon hybrid albumin fusion proteins areencompassed by the invention, as are host cells and vectors containingpolynucleotides encoding the polypeptides. In one embodiment, ainterferon hybrid albumin fusion protein encoded by a polynucleotide asdescribed above has extended shelf life. In an additional embodiment, ainterferon hybrid albumin fusion protein encoded by a polynucleotidedescribed above has a longer serum half-life and/or more stabilizedactivity in solution (or in a pharmaceutical composition) in vitroand/or in vivo than the corresponding unfused interferon hybridmolecule.

In another non-limiting example, a “Therapeutic protein” is a proteinthat has a biological activity, and in particular, a biological activitythat is useful for treating, preventing or ameliorating a disease. Anon-inclusive list of biological activities that may be possessed by aTherapeutic protein includes, enhancing the immune response, promotingangiogenesis, inhibiting angiogenesis, regulating endocrine function,regulating hematopoietic functions, stimulating nerve growth, enhancingan immune response, inhibiting an immune response, or any one or more ofthe biological activities described in the “Biological Activities”section below and/or as disclosed for a given Therapeutic protein inTable 1 (column 2).

As used herein, “therapeutic activity” or “activity” may refer to anactivity whose effect is consistent with a desirable therapeutic outcomein humans, or to desired effects in non-human mammals or in otherspecies or organisms. Therapeutic activity may be measured in vivo or invitro. For example, a desirable effect may be assayed in cell culture.As an example, when EPO is the Therapeutic protein, the effects of EPOon cell proliferation as described in Example 8 may be used as theendpoint for which therapeutic activity is measured. Such in vitro orcell culture assays are commonly available for many Therapeutic proteinsas described in the art. Examples of assays include, but are not limitedto those described herein in the Examples section or in the “ExemplaryActivity Assay” column (column 3) of Table 1.

Therapeutic proteins corresponding to a Therapeutic protein portion ofan albumin fusion protein of the invention, such as cell surface andsecretory proteins, are often modified by the attachment of one or moreoligosaccharide groups. The modification, referred to as glycosylation,can dramatically affect the physical properties of proteins and can beimportant in protein stability, secretion, and localization.Glycosylation occurs at specific locations along the polypeptidebackbone. There are usually two major types of glycosylation:glycosylation characterized by O-linked oligosaccharides, which areattached to serine or threonine residues; and glycosylationcharacterized by N-linked oligosaccharides, which are attached toasparagine residues in an Asn-X-Ser or Asn-X-Thr sequence, where X canbe any amino acid except proline. N-acetylneuramic acid (also known assialic acid) is usually the terminal residue of both N-linked and0-linked oligosaccharides. Variables such as protein structure and celltype influence the number and nature of the carbohydrate units withinthe chains at different glycosylation sites. Glycosylation isomers arealso common at the same site within a given cell type.

For example, several types of human interferon are glycosylated. Naturalhuman interferon-α2 is O-glycosylated at threonine 106, andN-glycosylation occurs at asparagine 72 in interferon-α14 (Adolf et al.,J. Biochem 276:511 (1991); Nyman T A et al., J. Biochem 329:295 (1998)).The oligosaccharides at asparagine 80 in natural interferon-β1α may playan important factor in the solubility and stability of the protein, butmay not be essential for its biological activity. This permits theproduction of an unglycosylated analog (interferon-β1b) engineered withsequence modifications to enhance stability (Hosoi et al., J. InterferonRes. 8:375 (1988; Karpusas et al., Cell Mol Life Sci 54:1203 (1998);Knight, J. Interferon Res. 2:421 (1982); Runkel et al., Pharm Res 15:641(1998); Lin, Dev. Biol. Stand. 96:97 (1998)). Interferon-γ contains twoN-linked oligosaccharide chains at positions 25 and 97, both importantfor the efficient formation of the bioactive recombinant protein, andhaving an influence on the pharmacokinetic properties of the protein(Sareneva et al., Eur. J. Biochem 242:191 (1996); Sareneva et al.,Biochem J. 303:831 (1994); Sareneva et al., J. Interferon Res. 13:267(1993)). Mixed O-linked and N-linked glycosylation also occurs, forexample in human erythropoietin, N-linked glycosylation occurs atasparagine residues located at positions 24, 38 and 83 while O-linkedglycosylation occurs at a serine residue located at position 126 (Lai etal., J. Biol. Chem. 261:3116 (1986); Broudy et al., Arch. Biochem.Biophys. 265:329 (1988)).

Glycosylation of EPO albumin fusion proteins may influence the activityand/or stability of the EPO albumin fusion proteins. The EPO portion ofthe albumin fusion protein may contain 3 N-linked sites forglycosylation, each of which can carry one tetra-antennary structure.When the EPO albumin fusion protein is glycosylated, the half-life ofthe molecule may be increased. In one embodiment, the EPO albumin fusionprotein is glycosylated. In another embodiment, the EPO albumin fusionprotein is hyperglycosylated.

One type of sugar commonly found in oligosaccharides is sialic acid.Each tetra-antennary structure of the N-linked glycosylation sites ofEPO may carry four sialic acid residues. Accordingly, in a preferredembodiment, the EPO albumin fusion protein is glycosylated with acarbohydrate group containing sialic acid. In an additional embodiment,the EPO albumin fusion protein comprises a fully sialylated EPO proteincontaining four sialic acid residues per tetra-antennerary structure persite with a molar ratio of sialic acid to protein 12:1 or greater. Inalternative embodiments, the EPO albumin fusion protein comprises ahypersialylated EPO protein wherein one, two, or three sialic acidresidues are attached at each tetra-antennerary structure per site witha molar ratio of sialic acid to protein less than 12:1.

Two types of sialic acid that may be used in the sialylation of the EPOalbumin fusion protein are N-acetylneuraminic acid (Neu5Ac) orN-glycolylneuraminic acid (Neu5Gc). In a preferred embodiment,hypersialylated EPO albumin fusion proteins contain Neu5Ac. Morepreferably, the total sialic acid content of hypersialylated EPO albuminfusion proteins is at least 97% Neu5Ac. Most preferred are EPO albuminfusion protein structures with little or no Neu5Gc.

Preferably, the albumin EPO fusion protein has at least 4 moles ofsialylation, and more preferably, at least 8-9 moles of sialylation. Anadditional embodiment comprises an albumin EPO fusion protein with 4moles of sialylation, 5 moles of sialylation, 6 moles of sialylation, 7moles of sialylation, 8-9 moles of sialylation, 8 moles of sialylation,9 moles of sialylation, 10 moles of sialylation, 11 moles ofsialylation, or 12 moles of sialylation.

The degree of sialylation of a protein changes the charge of the proteinand its retention time on a chromatography column. Therefore, certainchromatography steps used in the purification process may be used tomonitor or enrich for hypersialylated EPO albumin fusion proteins. In apreferred embodiment, the amount of sialylation may be monitored by HPLCchromatography. In an additional embodiment, steps in the purificationprocess of EPO albumin fusions may be used to enrich for hypersialylatedEPO albumin fusion proteins. In a preferred embodiment the purificationsteps that may be used to enrich for hypersialylated EPO albumin fusionproteins comprise the butyl-sepharose FF purification step to removevirus particles by high ammonium salt and the hydroxyapatitechromatography at pH 6.8 for the final purification step.

Therapeutic proteins corresponding to a Therapeutic protein portion ofan albumin fusion protein of the invention, as well as analogs andvariants thereof, may be modified so that glycosylation at one or moresites is altered as a result of manipulation(s) of their nucleic acidsequence, by the host cell in which they are expressed, or due to otherconditions of their expression. For example, glycosylation isomers maybe produced by abolishing or introducing glycosylation sites, e.g., bysubstitution or deletion of amino acid residues, such as substitution ofglutamine for asparagine, or unglycosylated recombinant proteins may beproduced by expressing the proteins in host cells that will notglycosylate them, e.g. in E. coli or glycosylation-deficient yeast.These approaches are described in more detail below and are known in theart.

Therapeutic proteins, particularly those disclosed in Table 1, and theirnucleic acid and amino acid sequences are well known in the art andavailable in public databases such as Chemical Abstracts ServicesDatabases (e.g., the CAS Registry), GenBank, and subscription provideddatabases such as GenSeq (e.g., Derwent). Exemplary nucleotide sequencesof Therapeutic proteins which may be used to derive a polynucleotide ofthe invention are shown in column 7, “SEQ ID NO:X,” of Table 2.Sequences shown as SEQ ID NO:X may be a wild type polynucleotidesequence encoding a given Therapeutic protein (e.g., either full lengthor mature), or in some instances the sequence may be a variant of saidwild type polynucleotide sequence (e.g., a polynucleotide which encodesthe wild type Therapeutic protein, wherein the DNA sequence of saidpolynucleotide has been optimized, for example, for expression in aparticular species; or a polynucleotide encoding a variant of the wildtype Therapeutic protein (i.e., a site directed mutant; an allelicvariant)). It is well within the ability of the skilled artisan to usethe sequence shown as SEQ ID NO:X to derive the construct described inthe same row. For example, if SEQ ID NO:X corresponds to a full lengthprotein, but only a portion of that protein is used to generate thespecific CID, it is within the skill of the art to rely on molecularbiology techniques, such as PCR, to amplify the specific fragment andclone it into the appropriate vector.

Additional Therapeutic proteins corresponding to a Therapeutic proteinportion of an albumin fusion protein of the invention include, but arenot limited to, one or more of the Therapeutic proteins or peptidesdisclosed in the “Therapeutic Protein X” column of Table 1 (column 1),or fragment or variable thereof

Table 1 provides a non-exhaustive list of Therapeutic proteins thatcorrespond to a Therapeutic protein portion of an albumin fusion proteinof the invention, or an albumin fusion protein encoded by apolynucleotide of the invention. The first column, “Therapeutic ProteinX,” discloses Therapeutic protein molecules that may be followed byparentheses containing scientific and brand names of proteins thatcomprise, or alternatively consist of, that Therapeutic protein moleculeor a fragment or variant thereof. “Therapeutic protein X” as used hereinmay refer either to an individual Therapeutic protein molecule, or tothe entire group of Therapeutic proteins associated with a givenTherapeutic protein molecule disclosed in this column. The “Biologicalactivity” column (column 2) describes Biological activities associatedwith the Therapeutic protein molecule. Column 3, “Exemplary ActivityAssay,” provides references that describe assays which may be used totest the therapeutic and/or biological activity of a Therapeuticprotein:X or an albumin fusion protein comprising a Therapeutic proteinX (or fragment thereof) portion. Each of the references cited in the“Exemplary Activity Assay” column are herein incorporated by referencein their entireties, particularly with respect to the description of therespective activity assay described in the reference (see Methodssection therein, for example) for assaying the corresponding biologicalactivity set forth in the “Biological Activity” column of Table 1. Thefourth column, “Preferred Indication: Y,” describes disease, disorders,and/or conditions that may be treated, prevented, diagnosed, and/orameliorated by Therapeutic protein X or an albumin fusion proteincomprising a Therapeutic protein X (or fragment thereof) portion. The“Construct ID” column (column 5) provides a link to an exemplary albuminfusion construct disclosed in Table 2 which encodes an albumin fusionprotein comprising, or alternatively consisting of the referencedTherapeutic Protein X (or fragment thereof) portion.

TABLE 1 Therapeutic Protein: X Biological Activity Exemplary ActivityAssay Preferred Indication: Y Construct ID Therapeutic Protein: Z EPOStimulates cellular Cell proliferation assay Anemia; Anemia in RenalDisease; Anemia in 1772, 1774, 1781, 1783, See Table 2, SEQ ID NO: Z(Erythropoietin; differentiation of bone- using a erythroleukemic cellOncology Patients; Bleeding Disorders; Chronic 1793, 1794, 1925, 1926,for particular construct. Epoetin alfa; marrow stem cells at an lineTF-1. (Kitamura et al. Renal Failure; Chronic Renal Failure in Pre-1966, 1969, 1980, 1981, Epoetin beta; early stage of 1989 J. Cell.Physiol. Dialysis Patients; Renal Disease; End-Stage 1994, 1995, 1996,1997, Gene-activated erythropoiesis; 140: 323) Renal Disease; End-StageRenal Disease in 2047, 2102, 2283, 2284, erythropoietin; accelerates theDialysis Patients; Chemotherapy; Chemotherapy 2287, 2289, 2294, 2298,Darbepoetin- proliferation and in Cancer Patients; Anemia inzidovudine-treated 2310, 2311, 2325, 2326, alpha; NESP; maturation ofterminally HIV patients; Anemia in zidovudine-treated 2344, 2363, 2373,2387, Epogen; Procrit; differentiating cells into patients; Anemia inHIV patients; Anemia in 2414, 2441, 2603, 2604, Eprex; Erypo;erythrocytes; and premature infants; Surgical patients (pre and/or 2605,3194, 3195, 3196, Espo; Epoimmun; modulates the level of post surgery);Surgical patients (pre and/or post EPOGIN; circulating erythrocytes.surgery) who are anemic; Surgical patients (pre NEORECORMON; and/or postsurgery) who are undergoing elective HEMOLINK; surgery; Surgicalpatients (pre and/or post Dynepo; surgery) who are undergoing elective,non- ARANESP) cardiac surgery; Surgical patients (pre and/or postsurgery) who are undergoing elective, non- cardiac, non-vascularsurgery; Surgical patients (pre and/or post surgery) who are undergoingelective, non-vascular surgery; Surgical patients (pre and/or postsurgery) who are undergoing cardiac and/or vascular surgery; Aplasticanemia; Refractory anemia; Anemia in Inflammatory Bowel Disease;Refractory anemia in Inflammatory Bowel Disease; Transfusion avoidance;Transfusion avoidance for surgical patients; Transfusion avoidance forelective surgical patients; Transfusion avoidance for electiveorthopedic surgical patients; Patients who want to Increase Red BloodCells. G-CSF Stimulates the Proliferation of murine Chemoprotection;Adjunct to Chemotherapy; 1642, 1643, 2363, 2373, See Table 2, SEQ ID NO:Z (Granulocyte proliferation and NFS-60 cells (Weinstein et Inflammatorydisorders; Cancer; Leukemia; 2387, 2414, 2441, 2702, for particularconstruct. colony- differentiation of the al, Proc Natl Acad Sci USAMyelocytic leukemia; Neutropenia, Primary 2637, 2700, 2701, 2703,stimulating factor; progenitor cells for 1986; 83, pp5010-4)neutropenias (e.g.; Kostmann syndrome); 2886, 2887, 2888, 2889,Granulokine; granulocytes and Secondary neutropenia; Prevention of 2890,KRN 8601; monocytes-macrophages. neutropenia; Prevention and treatmentof Filgrastim; neutropenia in HIV-infected patients; PreventionLenograstim; and treatment of neutropenia associated with Meograstim;chemotherapy; Infections associated with Nartograstim; neutropenias;Myelopysplasia; Autoimmune Neupogen; disorders; Psoriasis; Mobilizationof NOPIA; Gran; hematopoietic progenitor cells; Wound Healing;GRANOCYTE; Autoimmune Disease; Transplants; Bone marrow Granulokine;transplants; Acute myelogeneous leukemia; Neutrogin; Neu- Lymphoma,Non-Hodgkin's lymphoma; Acute up; Neutromax) lymphoblastic leukemia;Hodgkin's disease; Accelerated myeloid recovery; Glycogen storagedisease. GM-CSF Regulates hematopoietic Colony Stimulating Assay: BoneMarrow Disorders; Bone marrow 1697, 1699, 2066, and 2067. See Table 2,SEQ ID NO: Z (Granulocyte- cell differentiation, gene Testa, N. G., etal., “Assays transplant; Chemoprotection; Hepatitis C; HIV forparticular construct. macrophage expression, growth, and forhematopoietic growth Infections; Cancer; Lung Cancer; Melanoma; colony-function. factors.” Balkwill F R (edt) Malignant melanoma; Mycobacteriumavium stimulating factor; Cytokines, A practical complex; Mycoses;Leukemia; Myeloid rhuGM-CSF; BI Approach, pp 229-44; IRL Leukemia;Infections; Neonatal infections; 61012; Prokine; Press Oxford 1991.Neutropenia; Mucositis; Oral Mucositis; Prostate Molgramostim; Cancer;Stem Cell Mobilization; Vaccine Sargramostim; Adjuvant; Ulcers (such asDiabetic, Venous GM-CSF/IL 3 Stasis, or Pressure Ulcers); Prevention offusion; neutropenia; Acute myelogenous leukemia; Milodistim;Hematopoietic progenitor cell mobilization; Leucotropin; Lymphoma;Non-Hodgkin's lymphoma; Acute PROKINE; Lymphoblastic Leukemia; Hodgkin'sdisease; LEUKOMAX; Accelerated myeloid recovery; Transplant Interberin;Rejection; Xenotransplant Rejection. Leukine; Leukine Liquid; Pixykine)Human growth Binds to two GHR Ba/F3-hGHR proliferation Acromegaly;Growth failure; Growth hormone 3163, 2983, See Table 2, SEQ ID NO: Zhormone molecules and Induces assay, a novel specific replacement;Growth hormone deficiency; for particular construct. (Pegvisamont;signal transduction bioassay for serum human Pediatric Growth HormoneDeficiency; Adult Somatrem; through receptor growth hormone. J ClinGrowth Hormone Deficiency; Idiopathic Growth Somatropin; dimerizationEndocrinol Metab 2000 Hormone Deficiency; Growth retardation; TROVERT;November; 85(11): 4274-9 Prader-Willi Syndrome; Prader-Willi SyndromePROTROPIN; Plasma growth hormone in children 2 years or older; Growthdeficiencies; BIO-TROPIN; (GH) immunoassay and Growth failure associatedwith chronic renal HUMATROPE; tibial bioassay, Appl insufficiency;Osteoporosis; Postmenopausal NUTROPIN; Physiol 2000 osteoporosis;Osteopenia, Osteoclastogenesis; NUTROPIN AQ; December; 89(6): 2174-8burns; Cachexia; Cancer Cachexia; Dwarfism; NUTROPHIN; Growth hormone(hGH) Metabolic Disorders; Obesity; Renal failure; NORDITROPIN; receptormediated cell Turner's Syndrome; Fibromyalgia; Fracture GENOTROPIN;mediated proliferation, treatment; Frailty, AIDS wasting; Muscle SAIZEN;Growth Horm IGF Res 2000 Wasting; Short Stature; Diagnostic Agents;SEROSTIM) October; 10(5): 248-55 Female Infertility; lipodystrophy.International standard for growth hormone, Horm Res 1999; 51 Suppl 1:7-12 Insulin (Human Stimulates glucose uptake Insulin activity may beHyperglycemia; Diabetes; Diabetes Insipidus; 2250, 2255, 2276, 2278, SeeTable 2, SEQ ID NO: Z insulin; Insulin and promotes assayed in vitrousing a [3- Diabetes mellitus; Type 1 diabetes; Type 2 2656, 2668, 2669,2671, for particular construct. aspart; Insulin glycogenesis andH]-glucose uptake assay. (J diabetes; Insulin resistance; Insulindeficiency; 2821, 2822, 2832, 2877, Glargine; Insulin lipogenesis. BiolChem 1999 Oct. 22; Hyperlipidemia; Hyperketonemia; Non-insulin 2878,2882, 2885, 2891, lispro; Lys-B28 274(43): 30864-30873). dependentDiabetes Mellitus (NIDDM); Insulin- 2897, 2930, 2931, 2942, Pro-B29;lyspro; dependent Diabetes Mellitus (IDDM); A 2986, 3025, 3133, 3134, LY275585; Condition Associated With Diabetes Including, 3197, 3198, 2726,2727, diarginylinsulin; But Not Limited To Obesity, Heart Disease, 2784,2789 Des-B26-B30- Hyperglycemia, Infections, Retinopathy, And/Orinsulin-B25- Ulcers; Metabolic Disorders; Immune Disorders; amide;Insulin Obesity; Vascular Disorders; Suppression of detemir; LABI; BodyWeight; Suppression of Appetite; NOVOLIN; Syndrome X. NOVORAPID;HUMULIN; NOVOMIX 30; VELOSULIN; NOVOLOG; LANTUS; ILETIN; HUMALOG;MACRULIN; EXUBRA; INSUMAN; ORALIN; ORALGEN; HUMAHALE; HUMAHALIN)Interferon alfa Confers a range of Anti-viral assay: Rubinstein Viralinfections; HIV Infections; Hepatitis; 2249, 2343, 2366, 2381, See Table2, SEQ ID NO: Z (Interferon alfa- cellular responses S, Familletti P C,Pestka S. Chronic Hepatitis; Hepatitis B; Chronic Hepatitis 2382, 2410,and 3165. for particular construct. 2b; recombinant; includingantiviral, (1981) Convenient assay for B; Hepatitis C; Chronic HepatitisC; Hepatitis D; Interferon alfa-n1; antiproliferative, interferons. J.Virol. Chronic Hepatitis D; Human Papillomavirus; Interferon alfa-n3;antitumor and 37(2): 755-8; Anti- Herpes Simplex Virus Infection;External Peginterferon immunomodulatory proliferation assay: Gao Y,Condylomata Acuminata; HIV; HIV Infection; alpha-2b; activities;stimulate et al (1999) Sensitivity of Oncology; Cancer; Solid Tumors;Melanoma; Ribavirin and production of two an epstein-barr virus-Malignant Melanoma; Renal Cancer (e.g., Renal interferon alfa-2b;enzymes: a protein kinase positive tumor line, Daudi, Cell Carcinoma);Lung Cancer (e.g, . Non-Small Interferon and an oligoadenylate to alphainterferon correlates Cell Lung Cancer or Small Cell Lung Cancer)alfacon-1; synthetase. with expression of a GC- Colon Cancer; BreastCancer; Liver Cancer; interferon rich viral transcript. Mol ProstateCancer; Bladder Cancer; Gastric Cancer; consensus; YM Cell Biol. 19(11):7305-13. Sarcoma; AIDS-Related Kaposi's Sarcoma; 643; CIFN; Lymphoma; TCell Lymphoma; Cutaneous T- interferon -alpha Cell Lymphoma;Non-Hodgkin's Lymphoma; consensus; Brain Cancer; Glioma; GlioblastomaMultiforme; recombinant Cervical Dysplasia; Leukemia; Preleukemia;methionyl Bone Marrow Disorders; Bone Disorders; Hairy consensus CellLeukemia; Chronic Myelogeonus Leukemia; interferon; HematologicalMalignancies; Hematological recombinant Disorders; Multiple Myeloma;Bacterial consensus Infections; Chemoprotection; Thrombocytopenia;interferon; CGP Multiple Sclerosis; Pulmonary Fibrosis; Age- 35269; RORelated Macular Degeneration; Macular 253036; RO Degeneration; Crohn'sDisease; Neurological 258310; INTRON Disorders; Arthritis; RheumatoidArthritis; A; PEG- Ulcerative Colitis; Osteoporosis, Osteopenia, INTRON;OIF; Osteoclastogenesis; Fibromyalgia; Sjogren's OMNIFERON; Syndrome;Chronic Fatigue Syndrome; Fever; PEG- Hemmorhagic Fever; ViralHemmorhagic OMNIFERON; Fevers; Hyperglycemia; Diabetes; DiabetesVELDONA; Insipidus; Diabetes mellitus; Type 1 diabetes; PEG- Type 2diabetes; Insulin resistance; Insulin REBETRON; deficiency;Hyperlipidemia; Hyperketonemia; ROFERON A; Non-insulin dependentDiabetes Mellitus WELLFERON; (NIDDM); Insulin-dependent DiabetesMellitus ALFERON (IDDM); A Condition Associated With Diabetes N/LDO;Including, But Not Limited To Obesity, Heart REBETRON; Disease,Hyperglycemia, Infections, Retinopathy, ALTEMOL; And/Or Ulcers;Metabolic Disorders; Immune VIRAFERONPEG; Disorders; Obesity; VascularDisorders; PEGASYS; Suppression of Body Weight; Suppression of Appetite;VIRAFERON; Syndrome X. VIRAFON; AMPLIGEN; INFERGEN; INFAREX; ORAGEN)Calcitonin Regulates levels of Hypocalcemic Rat Bioassay, BoneDisorders; Fracture prevention; 1833, 1834, 1835, 1836, See Table 2, SEQID NO: Z (Salmon calcium and phosphate in bone resorbing assay andHypercalcemia; Malignant hypercalcemia; 2447, 2513, 2806, 2915 forparticular construct. Calcitonin serum; causes a reduction the pitassay, CT receptor Osteoporosis; Paget's disease; Osteopenia,(Salcatonin); in serum calcium--an binding assay, CAMPOsteoclastogenesis; osteolysis; osteomyelitis; Calcitonin effectopposite to that of stimulation assay: J Bone osteonecrosis; periodontalbone loss; human-salmon human parathyroid Miner Res 1999 osteoarthritis;rheumatoid arthritis; osteopetrosis; hybrid; hormone. August; 14(8):1425-31 periodontal, lytic, or metastatic bone disease; Forcaltonin;osteoclast differentiation inhibition; bone Fortical; disorders; bonehealing and regeneration. Calcitonin; Calcitonina Almirall; CalcitoninaHubber; Calcimar; Calsynar; Calogen; Miacalcic; Miacalcin; SB205614;Macritonin; Cibacalcin; Cibacalcina; Cibacalcine; Salmocalcin;PowderJect Calcitonin) (CAS-21215-62- 3) Interferon beta Modulates MHCantigen Anti-viral assay: Rubinstein Multiple Sclerosis; Oncology;Cancer; Solid 1778, 1779, 2011, 2013, See Table 2, SEQ ID NO: Z(Interferon beta- expression, NK cell S, Familletti P C, Pestka S.Tumors; Melanoma; Malignant Melanoma; Renal 2053, 2054, 2492, 2580, forparticular construct. 1a; Interferon activity and IFNg (1981) Convenientassay for Cancer (e.g., Renal Cell Carcinoma); Lung 2795, 2796, 2797.beta 1b; production and IL12 interferons. J. Virol. Cancer (e.g, .Non-Small Cell Lung Cancer or Interferon-beta- production in monocytes.37(2): 755-8; Anti- Small Cell Lung Cancer) Colon Cancer; Breast serine;SH 579; proliferation assay: Gao Y, Cancer; Liver Cancer; ProstateCancer; Bladder ZK 157046; et al (1999) Sensitivity of Cancer; GastricCancer; Sarcoma; AIDS-Related BCDF; beta-2 IF; an epstein-barr virus-Kaposi's Sarcoma; Lymphoma; T Cell Interferon-beta-2; positive tumorline, Daudi, Lymphoma; Cutaneous T-Cell Lymphoma; Non- rhIL-6; SJ0031;to alpha interferon correlates Hodgkin's Lymphoma; Brain Cancer; Glioma;DL 8234; with expression of a GC- Glioblastoma Multiforme; CervicalDysplasia; FERON; IFNbeta; rich viral transcript. Mol Leukemia;Preleukemia; Bone Marrow BETASERON; Cell Biol. 19(11): 7305-13.Disorders; Bone Disorders; Hairy Cell Leukemia; AVONEX; ChronicMyelogeonus Leukemia; Hematological REBIF; Malignancies; HematologicalDisorders; Multiple BETAFERON; Myeloma; Bacterial Infections; SIGOSIX)Chemoprotection; Thrombocytopenia; Viral infections; HIV Infections;Hepatitis; Chronic Hepatitis; Hepatitis B; Chronic Hepatitis B;Hepatitis C; Chronic Hepatitis C; Hepatitis D; Chronic Hepatitis D;Human Papillomavirus; Herpes Simplex Virus Infection; ExternalCondylomata Acuminata; HIV; HIV Infection; Pulmonary Fibrosis;Age-Related Macular Degeneration; Macular Degeneration; Crohn's Disease;Neurological Disorders; Arthritis; Rheumatoid Arthritis; UlcerativeColitis; Osteoporosis, Osteopenia, Osteoclastogenesis; Fibromyalgia;Sjogren's Syndrome; Chronic Fatigue Syndrome; Fever; Hemmorhagic Fever;Viral Hemmorhagic Fevers; Hyperglycemia; Diabetes; Diabetes Insipidus;Diabetes mellitus; Type 1 diabetes; Type 2 diabetes; Insulin resistance;Insulin deficiency; Hyperlipidemia; Hyperketonemia; Non-insulindependent Diabetes Mellitus (NIDDM); Insulin-dependent Diabetes Mellitus(IDDM); A Condition Associated With Diabetes Including, But Not LimitedTo Obesity, Heart Disease, Hyperglycemia, Infections, Retinopathy,And/Or Ulcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX. Growth hormone Acts on the anterior Growth hormone-releasingAcromegaly; Growth failure; Growth hormone 1747 and 1748. See Table 2,SEQ ID NO: Z releasing factor; pituitary to stimulate the peptides(GHRPs) are replacement; Growth hormone deficiency; for particularconstruct. Growth hormone production and secretion known to releasegrowth Pediatric Growth Hormone Deficiency; Adult releasing of growthhormone and hormone (GH) in vivo and Growth Hormone Deficiency;Idiopathic Growth hormone exert a trophic effect on in vitro by a directaction on Hormone Deficiency; Growth retardation; (Sermorelin the gland.receptors in anterior Prader-Willi Syndrome; Prader-Willi Syndromeacetate; pituitary cells. Biological in children 2 years or older;Growth deficiencies; Pralmorelin; activity can be measured in Growthfailure associated with chronic renal Somatorelin; cell lines expressinggrowth insufficiency; Osteoporosis; Osteopenia, Somatoliberin; hormonereleasing factor Osteoclastogenesis; Postmenopausal Geref; Gerel;receptor (Mol Endocrinol osteoporosis; burns; Cachexia; Cancer Cachexia;Groliberin) 1992 October; 6(10): 1734-44, Dwarfism; Metabolic Disorders;Obesity; Renal Molecular Endocrinology, failure; Turner's Syndrome;Fibromyalgia; Vol 7, 77-84). Fracture treatment; Frailty, AIDS wasting;Muscle Wasting; Short Stature; Diagnostic Agents; Female Infertility;lipodystrophy. IL-2 Promotes the growth of B T cell proliferation assayCancer; Solid Tumors; Metastatic Renal Cell 1757, 1758, 1812, 1813, SeeTable 2, SEQ ID NO: Z (Aldesleukin; and T cells and augments “Biologicalactivity of Carcinoma; Metastatic Melanoma; Malignant 1952, 1954, 2030,and 2031. for particular construct. interleukin-2 NK cell and CTL cellrecombinant human Melanoma; Melanoma; Renal Cell Carcinoma; fusiontoxin; T killing activity. interleukin-2 produced in Renal Cancer; LungCancer (e.g, . Non-Small cell growth Escherichia coli.” Science CellLung Cancer or Small Cell Lung Cancer); factor; 223: 1412-1415, 1984.Colon Cancer; Breast Cancer; Liver Cancer; PROLEUKIN; natural killer(NK) cell and Leukemia; Preleukemia; Hematological IMMUNACE; CTLcytotoxicity assay Malignancies; Hematological Disorders; Acute CELEUK;“Control of homeostasis of Myeloid Leukemia; Melanoma; MalignantONCOLIPIN 2; CD8+ memory T cells by Melanoma; Non-Hodgkin's Lymphoma;Ovarian MACROLIN) opposing cytokines. Science Cancer; Prostate Cancer;Brain Cancer; Glioma; 288: 675-678, 2000; CTLL- Glioblastoma Multiforme;Hepatitis; Hepatitis C; 2 Proliferation: Gillis et al Lymphoma; HIVInfection (AIDS); (1978) J. Immunol. 120, Inflammatory Bowel Disorders;Kaposi's 2027 Sarcoma; Multiple Sclerosis; Arthritis; RheumatoidArthritis; Transplant Rejection; Diabetes; Type 1 Diabetes Mellitus;Type 2 Diabetes. Parathyroid Acts in conjuction with Adenylyl cyclaseBone Disorders; Fracture prevention; 1749, 1750, 1853, 1854, See Table2, SEQ ID NO: Z hormone; calcitonin to control stimulation in ratHypercalcemia; Malignant hypercalcemia; 1889, 1906, 1907, 1914, forparticular construct. parathyrin (PTH; calcium and phosphateosteosarcoma cells, Osteoporosis; Paget's disease; Osteopenia, 1932,1938, 1941, 1949, Ostabolin; ALX1- metabolism; elevates ovariectomizedrat model of Osteoclastogenesis; osteolysis; osteomyelitis; 2021, 2022,2023, 2428, 11; hPTH 1-34; blood calcium level; osteoporosis: IUBMB Lifeosteonecrosis; periodontal bone loss; 2714, 2791, 2965, 2966. LY 333334;MN stimulates the activity of 2000 February; 49(2): 131-5osteoarthritis; rheumatoid arthritis; osteopetrosis; 10T; parathyroidosteocytes; enhances periodontal, lytic, or metastatic bone disease;hormone (1-31); absorption of Ca+/Pi from osteoclast differentiationinhibition; bone FORTEO; small intestine into blood; disorders; bonehealing and regeneration. PARATHAR) promotes reabsorption of Ca+ andinhibits Pi by kidney tubules. Resistin Mediates insulin Ability ofresistin to Hyperglycemia; Diabetes; Diabetes Insipidus; 2295, 2296,2297, 2300, See Table 2, SEQ ID NO: Z resistance in Type II influencetype II diabetes Diabetes mellitus; Type 1 diabetes; Type 2 and 2309.for particular construct. diabetes; inhibits insulin- can be determinedusing diabetes; Insulin resistance; Insulin deficiency; stimulatedglucose assays known in the art: Hyperlipidemia; Hyperketonemia;Non-insulin uptake Pontoglio et al., J Clin dependent Diabetes Mellitus(NIDDM); Insulin- Invest 1998 May dependent Diabetes Mellitus (IDDM); A15; 101(10): 2215-22. Condition Associated With Diabetes Including, ButNot Limited To Obesity, Heart Disease, Hyperglycemia, Infections,Retinopathy, And/Or Ulcers; Metabolic Disorders; Immune Disorders;Obesity; Vascular Disorders; Suppression of Body Weight; Suppression ofAppetite; Syndrome X. TR6 (DcR3; Inhibits Fas Ligand and Cellularapoptosis can be Fas Ligand or LIGHT induced apoptotic 1520, 1537, 1545,1546, See Table 2, SEQ ID NO: Z Decoy Receptor AIM-2 (TL5, LIGHT)measured by annexin disorders: hepatitis; liver failure (including 1568,1570, 1622, 1623, for particular construct. 3; FASTR) mediatedapoptosis. staining, TUNEL staining, fulminant liver failure); graftversus host 1645, 1700, 1702, 1703, measurement of caspase disease;graft rejection; myelodysplastic 1704, 1891, 1892, 1912, levels.Inhibition of cell syndrome; renal failure; insulin dependent and 1913.growth can also be directly diabetes mellitus; rheumatoid arthritis;measured, for example by inflammatory bowel disease; autoimmune ALOMARBlue staining. disease; toxic epidermal necrolysis; multiple Assay refs:cytotoxicity sclerosis. assay on human fibrosarcoma (Epsevik andNissen-Meyer, 1986, J. Immunol. methods). DeCAF (D- Inhibitsproliferation DeCAF activity can be B cell and/or T cell mediated immune1657. See Table 2, SEQ ID NO: Z SLAM; BCM- and differentiation of Bdetermined using assays disorders; Immunodeficiency (e.g., Common forparticular construct. like membrane cells; Antagonize BLyS known in theart, such as Variable Immunodeficiency, Selective IgA Deficiency)protein; activity for example, those BLAME (B described in Examples 32-lymphocyte 33 of International activator Publication No. macrophageWO0111046. expressed)) BLyS (B Promotes proliferation, BLyS activity canbe B cell and/or T cell mediated immune 1680, 2095, and 2096. See Table2, SEQ ID NO: Z Lymphocyte differentiation and determined using assaysdisorders, particularly immune system for particular construct.Stimulator; survival of B cells; known in the art, such as, disordersassociated with low B cell numbers Neutrokine Promotes for example, theor low serum immunoglobulin; alpha; TL7; immunoglobulin costimulatoryproliferation Immunodeficiency (e.g., Common Variable BAFF; TALL-production by B cells. assay and other assays Immunodeficiency,Selective IgA Deficiency). 1; THANK; disclosed by Moore et al.,Radiolabeled forms: lymphoma, non-Hodgkins radiolabeled 1999, Science,lymphoma, chronic lymphocytic leukemia, BLyS) 285(5425): 260-3. multiplemyeloma. Anti-BLyS Agonize or antagonize BLyS agonist or antagonist Bcell and/or T cell mediated immune 1821, 1956, 2501, 2502, See Table 2,SEQ ID NO: Z single chain BlyS activity. activity can be determineddisorders; Autoimmune disorders, particularly 2638. for particularconstruct. antibody using assays known in the autoimmune diseasesassociated with the (scFvI116A01, art, such as, for example, aproduction of autoantibodies; Rheumatoid scFvI050B11, modified versionthe Arthritis, Systemic Lupus Erythmatosus; scFvI006D08) costimulatoryproliferation Sjögren's Syndrome, cancers expressing Blys and others.assay disclosed by Moore et as an autocrine growth factor, e.g. certainal., 1999, Science, chronic lymphocytic leukemias. 285(5425): 260-3, inwhich BlyS is mixed or preincubated with the anti- BlyS antibody priorto being applied to the responder B lymphocytes. MPIF-1 Inhibits myeloidMPIF-1 activity can be Chemoprotection; Adjunct to Chemotherapy; 1681,3166, 3167, 3168, See Table 2, SEQ ID NO: Z (Myeloid progenitor cells;and measured using the Inflammatory disorders; Cancer; Leukemia; forparticular construct. Progenitor activates monocytes myeloprotectionassay and Myelocytic leukemia; Neutropenia, Primary Inhibitorychemotaxis assay described neutropenias (e.g.; Kostmann syndrome);Factor; in U.S. Pat. No. 6,001,606. Secondary neutropenia; Prevention ofCKbeta-8; neutropenia; Prevention and treatment of Mirostipen)neutropenia in HIV-infected patients; Prevention and treatment ofneutropenia associated with chemotherapy; Infections associated withneutropenias; Myelopysplasia; Autoimmune disorders; Psoriasis;Mobilization of hematopoietic progenitor cells; Wound Healing;Autoimmune Disease; Transplants; Bone marrow transplants; Acutemyelogeneous leukemia; Lymphoma, Non-Hodgkin's lymphoma; Acutelymphoblastic leukemia; Hodgkin's disease; Accelerated myeloid recovery;Glycogen storage disease. KDI Inhibits bone marrow KDI activity can beMultiple sclerosis; Hepatitis; Cancer; Viral 1746. See Table 2, SEQ IDNO: Z (Keratinocyte proliferation; and shows measured using theantiviral infections, HIV infections, Leukemia. for particularconstruct. Derived antiviral activity. and cell proliferation assaysInterferon; described in Examples 57- Interferon 63 of InternationalKappa Publication No. Precursor) WO0107608. TNFR2 (p75) Binds both TNFaand T-cell proliferation can be Autoimmune disease; RheumatoidArthritis; 1777 and 1784. See Table 2, SEQ ID NO: Z (ENBREL) TNFb;mediates T-cell measured using assays Psoriatic arthritis; Still'sDisease; Ankylosing for particular construct. proliferation by TNF;known in the art. For Spondylitis; Cardiovascular Diseases; reducessigns and example, “Lymphocytes: a Vasulitis; Wegener's granulomatosis;structural damage in practical approach” edited Amyloidosis; SystemicLupus Erythematosus, patients with by: S L Rowland, A JInsulin-Dependent Diabetes Mellitus; moderately to severly McMichael -chapter 6, Immunodeficiency Disorders; Infection; active rheumatoidpages 138-160 Oxford Inflammation; Inflammatory Bowel Disease; arthritis(RA). University Press (2000); Chrohn's Disease; Psoriasis; AIDS; Graftand “Current Protocols on Rejection; Graft Versus Host Disease. CD-ROM”section 3.12 Proliferation Assays for T- cell Function John Wiley &Soncs, Inc. (1999). Keratinocyte Stimulates epithelial KGF-2 activitycan be Stimulate Epithelial Cell Proliferation; 1785, 1786, 1916, 1917,See Table 2, SEQ ID NO: Z growth factor 2 cell growth. measured usingthe wound Stimulate Basal Keratinocytes; Wound 2498, 2499, 2552, 2553,for particular construct. (Repifermin; healing assays and Healing;Stimulate Hair Follicle Production; 2584, 2607, 2608, 2606, KGF-2;epithelial cell proliferation Healing Of Dermal Wounds. Wound Healing;2630 Fibroblast assays described in U.S. Eye Tissue Wounds, DentalTissue Wounds, Growth Factor- Pat. No. 6,077,692. Oral Cavity Wounds,Diabetic Ulcers, Dermal 10; FGF-10) Ulcers, Cubitus Ulcers, ArterialUlcers, Venous Stasis Ulcers, Burns Resulting From Heat Exposure OrChemicals, or Other Abnormal Wound Healing Conditions such as Uremia,Malnutrition, Vitamin Deficiencies or Complications Associated WithSystemic Treatment With Steroids, Radiation Therapy or AntineoplasticDrugs or Antimetabolites; Promote Dermal Reestablishment Subsequent ToDermal Loss; Increase the Adherence Of Skin Grafts To A Wound Bed;Stimulate Re- Epithelialization from The Wound Bed; To Promote SkinStrength; Improve The Appearance Of Aged Skin; Proliferate Hepatocytes,Lung, Breast, Pancreas, Stomach, Bladder, Small Intestine, LargeIntestine; Sebocytes, Hair Follicles, Type II Pneumocytes,Mucin-Producing Goblet Cells, or Other Epithelial Cells, EndothelialCells, Keratinocytes, or Basal Keratinocytes (and Their Progenitors)Contained Within The Skin, Lung, Liver, Bladder, Eye, Salivary Glands,or Gastrointestinal Tract; Reduce The Side Effects Of Gut Toxicity ThatResult From Radiation, Chemotherapy Treatments Or Viral Infections;Cytoprotector, especially of the Small Intestine Mucosa or Bladder;Mucositis (Mouth Ulcers); Regeneration Of Skin; Full and/or PartialThickness Skin Defects, including Burns, (e.g., Repopulation Of HairFollicles, Sweat Glands, And Sebaceous Glands); Psoriasis; EpidermolysisBullosa; Blisters; Gastric and/or Doudenal Ulcers; Reduce Scarring;Inflamamatory Bowel Diseases; Crohn's Disease; Ulcerative Colitis; GutToxicity; Lung Damage; Repair Of Alveoli And/or Brochiolar Epithelium;Acute Or Chronic Lung Damage; Emphysema, ARDS; Inhalation Injuries;Hyaline Membrane Diseases; Infant Respiratory Distress Syndrome;Bronchopulmonary Displasia In Premature Infants; Fulminant LiverFailure; Cirrhosis, Liver Damage caused by Viral Hepatitis and/or ToxicSubstances; Diabetes Mellitus; Inflammation. TR2 (and Inhibits B cellCo-stimulation B-cell Herpes; immune disorders; autoimmune 1788 and2129. See Table 2, SEQ ID NO: Z TR2sv1, proliferation, and proliferationassay and Ig disease; graft versus host disease; graft for particularconstruct. TR2SV2; mediates and inhibits production assay (Moore etrejection; variable immunodeficiency; TNFRSF14; Herpes Simplex Virusal., 1999, Science, immunodeficiency syndromes; cancer. HVEM; Herpes(HSV) infection. 285(5425): 260-3.). HSV-1 Virus Entry and HSV-2Infectivity Mediator; Assay: International ATAR) Publication No. WO97/04658 Macrophage Chemotactic for Chemokine activities can beInflammatory diseases; wound healing; 1809, 2137, 2474, 2475, See Table2, SEQ ID NO: Z derived monocyte-derived determined using assaysangiogenesis; AIDS infection. 2476, and 2477. for particular construct.chemokine, dendritic cells and IL-2- known in the art: Methods MDC(Ckbeta- activated natural killer in Molecular Biology, 13) cells. 2000,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot, T. N. C.Wells, and C. A. Power.  ©Humana Press Inc., Totowa, NJ HAGDG59Activates MIP1a Dendritic cell assays are Immune disorders; cancer;viral infection; 1830 and 1831. See Table 2, SEQ ID NO: Z (Retinalshort- release in Dendritic well known in the art. For inflammation;sepsis; arthritis; asthma. for particular construct. chain Cells.example, J. Immunol. dehydrogenase) 158: 2919-2925 (1997); J. Leukoc.Biol. 65: 822-828 (1999). GnRH Promotes release of GnRH is known tocause Infertility; Kallmann's syndrome or other forms 1862 and 1863. SeeTable 2, SEQ ID NO: Z (Gonadotropin follicle-stimulating the release offollicle of hypergonadotropic hypergonadism (failure for particularconstruct. Releasing hormone and luteinizing stimulating hormone (FSH)to go through puberty naturally). Hormone) hormone from anterior and/orluteinizing hormone pituitary. (LH) in vivo by a direct action onreceptors in anterior pituitary gonadotropes. GnRH activity can bedetermined by measuring FSH levels in the medium of culturedgonadotropes before and after GnRH supplementation. For example, Bakeret al. Biol Reprod 2000 September; 63(3): 865-71. Teprotide Inhibitsangiotensin Inhibition of ACE can be Hypertension; congestive heartfailure. 1866, 1867, 2025, and See Table 2, SEQ ID NO: Z convertingenzyme determined using assays 2026. for particular construct. (ACE).known in the art. For example, Anzenbacherova et al., J. Pharma BiomedAnal 2001 March; 24(5- 6): 1151-6. Human Involved in Chemokineactivities can be Autoimmune disorders; Immunity; Vascular 1933, 1934,1947, 1948, See Table 2, SEQ ID NO: Z chemokine inflammation, allergy,determined using assays and Inflammatory disorders; HIV; AIDS; 1955,1998, 2355, 2412, for particular construct. HCC-1 (ckBeta- tissuerejection, viral known in the art: Methods infectious diseases. 2449,2837, 2838, 2839, 1; HWFBD) infection, and tumor in Molecular Biology,2840, 2841, 2842, 2843, biology; enhances 2000, vol. 138: Chemokine2844, 2845, 2849, 2947, proliferation of CD34+ Protocols. Edited by: A.E. I. 3066, 3105, 3124, 3125, myeloid progenitor Proudfoot, T. N. C.Wells, 3139, 3152, 3153, 3154, cells. and C. A. Power.  ©Humana 3155,3156, 3169, 3170, Press Inc., Totowa, NJ 3202, 3203, 3204, 3205, 3206,3207, 3272 ACE2 inhibitor Inhibits production of Inhibition ofangiotensin Treatment for elevated angiotensin II and/or 1989, 2000,2001, and See Table 2, SEQ ID NO: Z (DX512) angiotensin II which can bedetermined using aldosterone levels, which can lead to 2002. forparticular construct. induces aldosterone assays known in the art.vasoconstriction, impaired cardiac output production, arteriolar Forexample, in vitro using and/or hypertension; Cardiovascular Disease; .smooth muscle a proliferation assay with Cardiac Failure; Diabetes; TypeII Diabetes; vasoconstriction, and rat cardiac fibroblasts asProteinuria; Renal disorders, congestive heart proliferation of cardiacdescribed in Naunyn failure. fibroblasts, Induces Schmiedebergs Archangiogenesis; an Pharmacol 1999 enzyme that converts May; 359(5): 394-9.angiotensin I to angiotensin1-9; also cleaves des-Arg, bradykinin andneurotensin. TR1 (OCIF; Inhibits Coculture Assay for Osteoporosis;Paget's disease; osteopenia; 2016, 2017, 2085, 2086, See Table 2, SEQ IDNO: Z Osteoclastogenesis osteoclastogenesis and Osteoclastogenesis, Boneosteolysis; osteomyelitis; osteonecrosis; 2529, 2530, 2531, 2532, forparticular construct. inhibitory bone resorption, and resorption assayusing fetal periodontal bone loss; osteoarthritis; 2555, 2556, 2557, andfactor; induces fibroblast long-bone organ culture rheumatoid arthritis;osteopetrosis; periodontal, 2558. osteoprotegerin, proliferation.system, dentine resorption lytic, or metastatic bone disease; osteoclastOPG; tumor assay, and fibroblast differentiation inhibition; bonedisorders; bone necrosis factor proliferation assays are healing andregeneration; organ calcification; receptor each described in Kwon etvascular calcification. superfamily al., FASEB J. 12: 845-854 member 11B(1998). precursor;) Human Chemotactic for both Chemokine activities canbe Cancer; Wound healing; Inflammatory 2101, 2240, 2241, 2245, See Table2, SEQ ID NO: Z chemokine activated (CD3+) T determined using assaysdisorders; Immmunoregulatory disorders; 2246, 2247, and 2248. forparticular construct. Ckbeta-7 cells and nonactivated known in the art:Methods Atherosclerosis; (CD14−) lymphocytes in Molecular Biology,Parasitic Infection; Rheumatoid Arthritis; and (CD4+) and 2000, vol.138: Chemokine Asthma; Autoimmune disorders. (CD8+) T lymphocytesProtocols. Edited by: A. E. I. and (CD45RA+) T cells Proudfoot, T. N. C.Wells, and C. A. Power.  ©Humana Press Inc., Totowa, NJ CKbeta4 Attractsand activates Chemokine activities can be Cancer; Solid Tumors; ChronicInfection; 2141, 2330, 2335, 2336, See Table 2, SEQ ID NO: Z (HGBAN46;microbicidal determined using assays Autoimmune Disorders; Psoriasis;Asthma; 2337, 2338, and 2348. for particular construct. HE9DR66)leukocytes; Attracts known in the art: Methods Allergy; Hematopoiesis;Wound Healing; Bone CCR6-expressing in Molecular Biology, MarrowFailure; Silicosis; Sarcoidosis; Hyper- immature dendritic cells 2000,vol. 138: Chemokine Eosinophilic Syndrome; Lung Inflammation; andmemory/effector T Protocols. Edited by: A. E. I. Fibrotic Disorders;Atherosclerosis; Periodontal cells; B-cell Proudfoot, T. N. C. Wells,diseases; Viral diseases; Hepatitis. chemotaxis; inhibits and C. A.Power.  ©Humana proliferation of myeloid Press Inc., Totowa, NJprogenitors; chemotaxis of PBMC's. Leptin Controls obesity in vivomodulation of food Hyperglycemia; Diabetes; Diabetes Insipidus; 2146,2184, 2186, and See Table 2, SEQ ID NO: Z through regulation of intake,reduction in body Diabetes mellitus; Type 1 diabetes; Type 2 2187. forparticular construct. appetite, reduction of weight, and lowering ofdiabetes; Insulin resistance; Insulin deficiency; body weight, andinsulin and glucose levels Hyperlipidemia; Hyperketonemia; Non-insulinlowering of insulin and in ob/ob mice, dependent Diabetes Mellitus(NIDDM); glucose level. radioimmunoassay (RIA) Insulin-dependentDiabetes Mellitus (IDDM); a and activation of the leptin ConditionAssociated With Diabetes Including, receptor in a cell-based But NotLimited To Obesity, Heart Disease, assay. Protein Expr PurifHyperglycemia, Infections, Retinopathy, 1998 December; 14(3): 335-42And/Or Ulcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX; Immunological Disorders; Immunosuppression. IL-1 receptor Binds IL1receptor 1) Competition for IL-1 Autoimmune Disease; Arthritis;Rheumatoid 2181, 2182, 2183, and See Table 2, SEQ ID NO: Z antagonistwithout activating the binding to IL-1 receptors in Arthritis; Asthma;Diabetes; Diabetes Mellitus; 2185. for particular construct. (Anakinra;target cells; inhibits the YT-NCI or C3H/HeJ cells GVHD; InflammatoryBowel Disorders; soluble binding of IL1-alpha (Carter et al., Nature344: Chron's Disease; Ocular Inflammation; interleukin-1 and IL1-beta;and 633-638, 1990); Psoriasis; Septic Shock; Transplant Rejection;receptor; IRAP; neutralizes the biologic 2) Inhibition of IL-1-Inflammatory Disorders; Rheumatic Disorders; KINERET; activity ofIL1-alpha induced endothelial cell- Osteoporosis; PostmenopausalOsteoporosis; ANTRIL) and IL1-beta. leukocyte adhesion (Carter Stroke.et al., Nature 344: 633-638, 1990); 3) Proliferation assays on A375-C6cells, a human melanoma cell line highly susceptible to theantiproliferative action of IL-1 (Murai T et al., J. Biol. Chem. 276:6797-6806, 2001). TREM-1 Mediates activation of Secretion of cytokines,Inflammation; Sepsis; bacterial infection; 2226 and 2230. See Table 2,SEQ ID NO: Z (Triggering neutrophil and chemokines, degranulation,autoimmune diseases; GVHD. for particular construct. Receptor monocytes;Stimulates and cell surface activation Expressed on neutrophil andmarkers can be determined Monocytes 1) monocyte-mediated using assaysdescribed in inflammatory response; Bouchon et al, J Immunol Promotessecretion of 2000 May TNF, IL-8, and MCP-1; 15; 164(10): 4991-5. Inducesneutrophil degranulation, Ca2+ mobilization and tyrosine phosphorylationof extracellular signal- related kinase 1 (ERK1), ERK2 and phospholipaseC- gamma. HCNCA73 Induces T-cell FMAT can be used to Autoimmunedisorders; Inflammation of the 2244 and 2365. See Table 2, SEQ ID NO: Zactivation- expression measure T-cell surface gastrointestinal tract;Cancer; Colon Cancer; for particular construct. of CD152 marker; markers(CD69, CD152, Allergy; Crohn's disease. Stimulates release of CD71,HLA-DR) and T-cell TNF-a and MIP-1a cytokine production (e.g., fromimmature, IFNg production). J. of monocyte-derived Biomol. Screen. 4:193-204 dendritic cells; (1999). Other T-cell Promotes maturation ofproliferation assays: dendritic cells. “Lymphocytes: a practicalapproach” edited by: S L Rowland, A J McMichael - Chapter 6, pages138-160 Oxford University Press (2000); WO 01/21658 Examples 11-14,16-17 and 33. VEGF-2 Promotes endothelial VEGF activity can be Coronaryartery disease; Critical limb 2251, 2252, 2256, and See Table 2, SEQ IDNO: Z (Vascular cell proliferation. determined using assays ischemia;Vascular disease; proliferation of 2257. for particular construct.Endothelial known in the art, such as endothelial cells, both vascularand lymphatic. Growth Factor- those disclosed in Antagonists may beuseful as anti-angiogenic 2; VEGF-C) International Publication agents;Cancer. No. WO0045835, for example. HCHNF25 Activates MIP1a Dendriticcell assays are Immune disorders; cancer. 2271, 2280, and 2320. SeeTable 2, SEQ ID NO: Z (jumping Release in Dendritic well known in theart. For for particular construct. translocation Cells. example, J.Immunol. breakpoint) 158: 2919-2925 (1997); J. Leukoc. Biol. 65: 822-828(1999). HLDOU18 Activates L6/GSK3 Assays for activation ofHyperglycemia; Diabetes; Diabetes Insipidus; 2328, 2340, 2350, 2351,SSee Table 2, SEQ ID NO:Z (Bone kinase assay. GSK3 kinase activity areDiabetes mellitus; Type 1 diabetes; Type 2 2359, 2362, 2367, 2369, forparticular construct. Morphogenic well known in the art. For diabetes;Insulin resistance; Insulin deficiency; 2370, 2473, Protein 9 example,Biol. Chem. Hyperlipidemia; Hyperketonemia; Non-insulin 2623, 2624,(BMP9); 379(8-9): (1998) 1101- dependent Diabetes Mellitus (NIDDM);Insulin- 2625, 2631, Growth 1110.; Biochem J. 1993 dependent DiabetesMellitus (IDDM); A 2632, 2633. differentiation Nov. 15; 296 (Pt 1):15-9. Condition Associated With Diabetes Including, factor-2 But NotLimited To Obesity, Heart Disease, precursor Hyperglycemia, Infections,Retinopathy, (GDF-2 And/Or Ulcers; Metabolic Disorders; Immuneprecursor)) Disorders; Obesity; Vascular Disorders; Suppression of BodyWeight; Suppression of Appetite; Syndrome X. Glucagon-Like- Stimulatesthe synthesis GLP1 activity may be Hyperglycemia; Diabetes; DiabetesInsipidus; 2448, 2455, 2456, 2457, See Table 2, SEQ ID NO: Z Peptide 1(GLP1; and release of insulin; assayed in vitro using a [3- Diabetesmellitus; Type 1 diabetes; Type 2 2803, 2804, 2900, 2904, for particularconstruct. Insulinotropin) enhances the sensitivity H]-glucose uptakeassay. (J diabetes; Insulin resistance; Insulin deficiency; 2945, 2964,2982, 3070, of adipose, muscle, and Biol Chem 1999 Oct. 22;Hyperlipidemia; Hyperketonemia; Non-insulin 2802, 3027, 3028, 3045,liver tissues towards 274(43): 30864-30873). dependent Diabetes Mellitus(NIDDM); Insulin- 3046, 3069, 3071, 3072, insulin; stimulates dependentDiabetes Mellitus (IDDM); A 3085, 3086, 3087, 3140, glucose uptake;slows the Condition Associated With Diabetes Including, 3309 digestiveprocess; But Not Limited To Obesity, Heart Disease, suppresses appetite;Hyperglycemia, Infections, Retinopathy, And/Or blocks the secretion ofUlcers; Metabolic Disorders; Immune Disorders; glucagon. Obesity;Vascular Disorders; Suppression of Body Weight; Suppression of Appetite;Syndrome X. Exendin-4 (AC- Stimulates the synthesis Exendin-4 activitymay be Hyperglycemia; Diabetes; Diabetes Insipidus; 2469 and 2470. SeeTable 2, SEQ ID NO: Z 2993) and release of insulin; assayed in vitrousing a [3- Diabetes mellitus; Type 1 diabetes; Type 2 for particularconstruct. enhances the sensitivity H]-glucose uptake assay. (Jdiabetes; Insulin resistance; Insulin deficiency; of adipose, muscle,and Biol Chem 1999 Oct. 22; Hyperlipidemia; Hyperketonemia; Non-insulinliver tissues towards 274(43): 30864-30873). dependent Diabetes Mellitus(NIDDM); Insulin- insulin; stimulates dependent Diabetes Mellitus(IDDM); A glucose uptake; slows the Condition Associated With DiabetesIncluding, digestive process; But Not Limited To Obesity, Heart Disease,suppresses appetite; Hyperglycemia, Infections, Retinopathy, And/Orblocks the secretion of Ulcers; Metabolic Disorders; Immune Disorders;glucagon. Obesity; Vascular Disorders; Suppression of Body Weight;Suppression of Appetite; Syndrome X. T20 (T20 HIV a peptide fromresidues Virus inhibition assays as HIV; AIDS; SIV (simianimmunodeficiency 7777, 2672, 2673 See Table 2, SEQ ID NO: Z inhibitory643-678 of the HIV gp41 described in Zhang et al., virus) infection. forparticular construct. peptide, DP178; transmembrane protein Sep. 26,2002, DP178 HIV ectodomain which binds Sciencexpress inhibitory to gp41in its resting state (www.sciencexpress.org). peptide) and preventstransformation to the fusogenic state T1249 (T1249 a second generationHIV Virus inhibition assays as HIV; AIDS; SIV (simian immunodeficiency9999, 2667, 2670, 2946 See Table 2, SEQ ID NO: Z HIV inhibitory fusioninbitor described in Zhang et al., virus) infection for particularconstruct. peptide; T1249 Sep. 26, 2002, anti-HIV peptide) Sciencexpress(www.sciencexpress.org). Interferon Confers a range of Anti-viral assay:Rubinstein Viral infections; HIV Infections; Hepatitis; 2875, 2872,2876, 2874, See Table 2, SEQ ID NO: Z Hybrids, cellular responses S,Familletti P C, Pestka S. Chronic Hepatitis; Hepatitis B; ChronicHepatitis 2873. for particular construct. specifically includingantiviral, (1981) Convenient assay for B; Hepatitis C; Chronic HepatitisC; Hepatitis D; preferred: antiproliferative, interferons. J. Virol.Chronic Hepatitis D; Human Papillomavirus; IFNalpha A/D antitumor and37(2): 755-8; Anti- Herpes Simplex Virus Infection; External hybrid(BgIII immunomodulatory proliferation assay: Gao Y, CondylomataAcuminata; HIV; HIV Infection; version) activities; stimulate et al(1999) Sensitivity of Oncology; Cancer; Solid Tumors; Melanoma; IFNalphaA/D production of two an epstein-barr virus- Malignant Melanoma; RenalCancer (e.g., Renal hybrid (PvuII enzymes: a protein kinase positivetumor line, Daudi, Cell Carcinoma); Lung Cancer (e.g, . Non-Smallversion) and an oligoadenylate to alpha interferon correlates Cell LungCancer or Small Cell Lung Cancer) IFNalpha A/F synthetase. Also, withexpression of a GC- Colon Cancer; Breast Cancer; Liver Cancer; hybridmodulates MHC antigen rich viral transcript. Mol Prostate Cancer;Bladder Cancer; Gastric Cancer; IFNalpha A/B expression, NK cell CellBiol. 19(11): 7305-13. Sarcoma; AIDS-Related Kaposi's Sarcoma; hybridactivity and IFNg Lymphoma; T Cell Lymphoma; Cutaneous T- IFNbeta1/alpha production and IL12 Cell Lymphoma; Non-Hodgkin's Lymphoma; Dhybrid production in monocytes. Brain Cancer; Glioma; GlioblastomaMultiforme; (IFNbeta-1/alpha- Cervical Dysplasia; Leukemia; Preleukemia;1 hybrid) Bone Marrow Disorders; Bone Disorders; Hairy IFNalpha/betaCell Leukemia; Chronic Myelogeonus Leukemia; hybrid HematologicalMalignancies; Hematological Disorders; Multiple Myeloma; BacterialInfections; Chemoprotection; Thrombocytopenia; Multiple Sclerosis;Pulmonary Fibrosis; Age- Related Macular Degeneration; MacularDegeneration; Crohn's Disease; Neurological Disorders; Arthritis;Rheumatoid Arthritis; Ulcerative Colitis; Osteoporosis, Osteopenia,Osteoclastogenesis; Fibromyalgia; Sjogren's Syndrome; Chronic FatigueSyndrome; Fever; Hemmorhagic Fever; Viral Hemmorhagic Fevers;Hyperglycemia; Diabetes; Diabetes Insipidus; Diabetes mellitus; Type 1diabetes; Type 2 diabetes; Insulin resistance; Insulin deficiency;Hyperlipidemia; Hyperketonemia; Non-insulin dependent Diabetes Mellitus(NIDDM); Insulin-dependent Diabetes Mellitus (IDDM); A ConditionAssociated With Diabetes Including, But Not Limited To Obesity, HeartDisease, Hyperglycemia, Infections, Retinopathy, And/Or Ulcers;Metabolic Disorders; Immune Disorders; Obesity; Vascular Disorders;Suppression of Body Weight; Suppression of Appetite; Syndrome X. B-typenatriuretic stimulates smooth muscle Inhibition of angiotensin canCongestive heart failure; cardiac volume 3119, 8888. See Table 2, SEQ IDNO: Z peptide (BNP, relaxation and be determined using assays overload;cardiac decompensation; Cardiac for particular construct. brainnatriuretic vasodilation, known in the art, for Failure; LeftVentricular Dysfunction; Dyspnea peptide) natriuresis, and example usingan in vitro suppression of renin- proliferation assay with ratangiotensin and cardiac fibroblasts as endothelin. described in NaunynSchmiedebergs Arch Pharmacol 1999 May; 359(5): 394-9. Vasodilation canbe measured in animals by measuring the myogenic responses of smallrenal arteries in an isobaric arteriograph system (see Am J PhysiolRegul Integr Comp Physiol 2002 August; 283(2): R349-R355). Natriuesis isdetermined by measuring the amount of sodium in the urine. α-defensin,Suppression of HIV Virus inhibition assays as HIV, AIDS; ARC. 3208,3209, 3210. See Table 2, SEQ ID NO: Z including alpha 1 replication;active against described in Zhang et al., for particular construct.defensin, alpha 2 bacteria, fungi, and Sep. 26, 2002, defensin, alpha 3enveloped viruses. Sciencexpress defensin (www.sciencexpress.org).(myeloid-related defensin; DEFA1; neutrophil- specific defensin; CAF)Phosphatonin Regulation of phosphate Blood phosphate levels canHyperphosphatemia; Hyperphosphatemia in 3238. See Table 2, SEQ ID NO: Z(matrix metabolism. be measured using methods chronic renal failure;hypophosphatemia; for particular construct. extracellular known in theart such as the Osteomalacia; Rickets; X-linked dominantphosphoglycoprotein; Hypophosphatemic Rat hypophosphatemicrickets/osteomalacia (XLH); MEPE) Bioassay. Zoolog Sci 1995 autosomaldominant hypophosphatemic October; 12(5): 607-10. rickets/osteomalacia(ADHR); tumor-induced rickets/osteomalacia (TIO). P1pal-12 Regulation ofprotease- Platelet aggregation can be Protection against systemicplatelet activation, 3274. See Table 2, SEQ ID NO: Z (pepducin,activated receptor (PAR) measured using methods thrombus, heart attack,stroke, and/or coagulation for particular construct. PAR1-based signaltransduction and known in the art such as disorders. pepducin)thrombin-mediated described in Nature aggregation of human Medicine 2002October; 8(10): platelets. 1161-1165. P4pal-10 Regulation of protease-Platelet aggregation can be Protection against systemic plateletactivation, 3275. See Table 2, SEQ ID NO: Z (pepducin, PAR4- activatedreceptor (PAR) measured using methods thrombus, heart attack, stroke,and/or coagulation for particular construct. based pepducin) signaltransduction and known in the art such as disorders. thrombin-mediateddescribed in Nature aggregation of human Medicine 2002 October; 8(10):platelets. 1161-1165. HRDFD27 Involved in the T-cell proliferation canbe Chemoprotection; Adjunct to Chemotherapy; 2361 See Table 2, SEQ IDNO: Z proliferation of T cells; measured using assays Inflammatorydisorders; Cancer; Leukemia; for particular construct. Production ofknown in the art. For Myelocytic leukemia; Neutropenia, PrimaryTNFgamma. example, “Lymphocytes: a neutropenias (e.g.; Kostmannsyndrome); practical approach” edited Secondary neutropenia; Preventionof by: S L Rowland, A J neutropenia; Prevention and treatment ofMcMichael - chapter 6, neutropenia in HIV-infected patients; Preventionpages 138-160 Oxford and treatment of neutropenia associated withUniversity Press (2000); and chemotherapy; Infections associated with“Current Protocols on CD- neutropenias; Myelopysplasia; Autoimmune ROM”section 3.12 disorders; Psoriasis; Mobilization of Proliferation Assaysfor T- hematopoietic progenitor cells; Wound Healing; cell Function JohnWiley & Autoimmune Disease; Transplants; Bone marrow Soncs, Inc. (1999).transplants; Acute myelogeneous leukemia; Lymphoma, Non-Hodgkin'slymphoma; Acute lymphoblastic leukemia; Hodgkin's disease; Acceleratedmyeloid recovery; Glycogen storage disease HWHGZ51 Stimulates an immuneThe ability to affect Skeletal diseases and disorders; Musculoskeletal2407, 2408 See Table 2, SEQ ID NO: Z (CD59; response and induceschondrocyte differentiation diseases and disorders; Bone fracturesand/or for particular construct. Metastasis- inflammation by inducingcan be measured using breaks; Osteoporosis (postmenopausal, senile, orassociated GPI- mononuclear cell, methods known in the art, idiopathicjuvenile); Gout and/or pseudogout; adhered protein eosinophil and PMNsuch as described in Bone Paget's disease; Osteoarthritis; Tumors and/orhomolog) infiltration; Inhibits (1995) September; 17(3): 279-86. cancersof the bone (osteochondromas, benign growth of breast cancer,chondromas, chondroblastomas, chondromyxoid ovarian cancer, leukemia,fibromas, osteoid osteomas, giant cell tumors, and melanoma; multiplemyelomas, osteosarcomas, Overexpressed in colon, fibrosarcomas,malignant fibrous histiocytomas, lung, breast and rectalchondrosarcomas, Ewing's tumors, and/or tumors; Regulates malignantlymphomas); Bone and joint infections glucose and/or FFA (osteomyelititsand/or infectious arthritis); update by adipocytes and Charcot's joints;Heel spurs; Sever's disease; skeletal muscle; Induces Sport's injuries;Cancer; Solid Tumors; redifferentiation of Melanoma; Malignant Melanoma;Renal Cancer chondrocytes (e.g., Renal Cell Carcinoma); Lung Cancer(e.g,. Non-Small Cell Lung Cancer or Small Cell Lung Cancer) ColonCancer; Breast Cancer; Liver Cancer; Prostate Cancer; Bladder Cancer;Gastric Cancer; Sarcoma; AIDS-Related Kaposi's Sarcoma; Lymphoma; T CellLymphoma; Cutaneous T-Cell Lymphoma; Non-Hodgkin's Lymphoma; BrainCancer; Glioma; Glioblastoma Multiforme; Cervical Dysplasia; Leukemia;Preleukemia; Bone Marrow Disorders; Bone Disorders; Hairy Cell Leukemia;Chronic Myelogeonus Leukemia; Hematological Malignancies; HematologicalDisorders; Multiple Myeloma; Kidney diseases and disorders;Shonlein-Henoch purpura, Berger disease, celiac disease, dermatitisherpetiformis, Chron disease; Diabetes; Diabetes Insipidus; Diabetesmellitus; Type 1 diabetes; Type 2 diabetes; Insulin resistance; Insulindeficiency; Hyperlipidemia; Hyperketonemia; Non-insulin dependentDiabetes Mellitus (NIDDM); Insulin-dependent Diabetes Mellitus (IDDM); ACondition Associated With Diabetes Including, But Not Limited ToObesity, Heart Disease, Hyperglycemia, Infections, Retinopathy, And/OrUlcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX; Kidney disorders; Hyperinsulinemia; Hypoinsulinemia; Immunologicaldisorders (e.g. arthritis, asthma, immunodeficiency diseases, AIDS,rheumatoid arthritis, granulomatous disease, inflammatory bowl disease,sepsis, acne, neutropenia, neutrophilia, psoriasis, hypersensitivities,T-cell mediated cytotoxicity, host-versus-graft disease, autoimmunitydisorders, demyelination, systemic lupus erythematosis, drug inducedhemolytic anemia, rheumatoid arthritis, Sjorgren's disease, scleroderma)C17 (cytokine- Inhibits glucose and/or Proliferation of kidney Kidneydiseases and disorders; Shonlein-Henoch 2489, 2490 See Table 2, SEQ IDNO: Z like protein C17) FFA uptake by mesangial cells can be purpura,Berger disease, celiac disease, for particular construct. adipocytes;Induces assayed using techniques dermatitis herpetiformis, Chrondisease; proliferation of kidney described in J. Investig. Diabetes;Diabetes Insipidus; Diabetes mellitus; mesangial cells; Med. (1998)August; Type 1 diabetes; Type 2 diabetes; Insulin Regulation of cytokine46(6): 297-302. resistance; Insulin deficiency; Hyperlipidemia;production and antigen Hyperketonemia; Non-insulin dependentpresentation Diabetes Mellitus (NIDDM); Insulin-dependent DiabetesMellitus (IDDM); A Condition Associated With Diabetes Including, But NotLimited To Obesity, Heart Disease, Hyperglycemia, Infections,Retinopathy, And/Or Ulcers; Metabolic Disorders; Immune Disorders;Obesity; Vascular Disorders; Suppression of Body Weight; Suppression ofAppetite; Syndrome X; Kidney disorders; Hyperinsulinemia;Hypoinsulinemia; Hematopoietic disorders; Immunological diseases anddisorders; Developmental diseases and disorders; Hepatic diseases anddisorders; Cancer (particularly leukemia); Immunological disorders (e.g.arthritis, asthma, immunodeficiency diseases, AIDS, rheumatoidarthritis, granulomatous disease, inflammatory bowl disease, sepsis,acne, neutropenia, neutrophilia, psoriasis, hypersensitivities, T-cellmediated cytotoxicity, host-versus-graft disease, autoimmunitydisorders, demyelination, systemic lupus erythematosis, drug inducedhemolytic anemia, rheumatoid arthritis, Sjorgren's disease, scleroderma)HDPBQ71 Regulates production and Such assays that may be Blood disordersand infection (e.g., viral 2515, 2545 See Table 2, SEQ ID NO: Zsecretion of IFNgamma; used or routinely modified infections,tuberculosis, infections associated for particular construct. Activationof myeloid to test immunomodulatory with chronic granulomatosus diseaseand cells and/or hematopoietic activity of polypeptides of malignantosteoporosis); Autoimmune disease cells the invention (including (e.g.,rheumatoid arthritis, systemic lupus antibodies and agonists orerythematosis, multiple sclerosis); antagonists of the invention)Immunodeficiency, boosting a T cell-mediated include the assaysdisclosed immune response, and suppressing a T cell- in Miraglia et al.,J mediated immune response; Inflammation and Biomolecular Screeninginflammatory disorders; Idiopathic pulmonary 4: 193-204 (1999); Rowlandfibrosis; Neoplastic diseases (e.g., leukemia, et al., ““Lymphocytes: alymphoma, melanoma); Neoplasms and cancers, practical approach”” suchas, for example, leukemia, lymphoma, Chapter 6: 138-160 (2000);melanoma, and prostate, breast, lung, colon, Gonzalez et al., J Clin Labpancreatic, esophageal, stomach, brain, liver and Anal 8(5): 225-233(1995); urinary cancer;. Benign dysproliferative disorders Billiau etal., Ann NY Acad and pre-neoplastic conditions, such as, for Sci 856:22-32 (1998); example, hyperplasia, metaplasia, and/or Boehm et al.,Annu Rev dysplasia; Anemia; Pancytopenia; Leukopenia; Immunol 15:749-795 Thrombocytopenia; Hodgkin's disease; Acute (1997), andRheumatology lymphocytic anemia (ALL); Plasmacytomas; (Oxford) 38(3):214-20 Multiple myeloma; Burkitt's lymphoma; (1999) Arthritis; AIDS;Granulomatous disease; Inflammatory bowel disease; Sepsis; Neutropenia;Neutrophilia; Psoriasis; Suppression of immune reactions to transplantedorgans and tissues; Hemophilia; Hypercoagulation; Diabetes mellitus;Endocarditis; Meningitis; Lyme Disease; Asthma; Allergy Oscar(osteoclast- Regulator of osteoclast Assay to detect osteoclast Skeletaldiseases and disorders; Musculo skeletal 2571, 2749 See Table 2, SEQ IDNO: Z associated differentiation; regulator differentiation is describeddiseases and disorders; Bone fractures and/or for particular construct.receptor isoform- of innate and adaptive in J. Exp. Med. (2002) Jan.breaks; Osteoporosis (postmenopausal, senile, or 3) immune responses 21;195(2): 201-9. idiopathic juvenile); Gout and/or pseudogout; Paget'sdisease; Osteoarthritis; Tumors and/or cancers of the bone(osteochondromas, benign chondromas, chondroblastomas, chondromyxoidfibromas, osteoid osteomas, giant cell tumors, multiple myelomas,osteosarcomas, fibrosarcomas, malignant fibrous histiocytomas,chondrosarcomas, Ewing's tumors, and/or malignant lymphomas); Bone andjoint infections (osteomyelitits and/or infectious arthritis); Charcot'sjoints; Heel spurs; Sever's disease; Sport's injuries Tumstatin (T5, T7Inhibits angiogenesis; A tumor cell proliferation Cancer; Solid Tumors;Melanoma; Malignant 2647, 2648, 2649, 2650, See Table 2, SEQ ID NO: Z orT8 peptide; Inhibits tumor growth; assay is described in J. Biol.Melanoma; Renal Cancer (e.g., Renal Cell 2943, 2944, 3047, 3048 forparticular construct. α3(IV)NC1) Inhibits protein synthesis Chem. (1997)272: 20395- Carcinoma); Lung Cancer (e.g, . Non-Small Cell 20401. LungCancer or Small Cell Lung Cancer) Colon Protein synthesis can be Cancer;Breast Cancer; Liver Cancer; Prostate measured as described in Cancer;Bladder Cancer; Gastric Cancer; Science (2002) Jan. 4; Sarcoma;AIDS-Related Kaposi's Sarcoma; 295(5552): 140-3. Lymphoma; T CellLymphoma; Cutaneous T- Cell Lymphoma; Non-Hodgkin's Lymphoma; BrainCancer; Glioma; Glioblastoma Multiforme; Cervical Dysplasia; Leukemia;Preleukemia; Bone Marrow Disorders; Bone Disorders; Hairy Cell Leukemia;Chronic Myelogeonus Leukemia; Hematological Malignancies; HematologicalDisorders; Multiple Myeloma; Angiogenesis CNTF (Ciliary Enhances myelinRegulation of myelin Neurological and neural diseases and disorders,2724, 2725, 3171, 3172 See Table 2, SEQ ID NO: Z neurotrophic formation;Reduces formation can be assayed as particularly diseases and disordersassociated for particular construct. factor) photoreceptor described inJ. Neurosci. with myelin and demyelination, such as, for degredation;Regulates (2002) Nov. 1; 22(21): 9221- example, ALS, multiple sclerosis,Huntington's calcium currents 7. disease; Neuronal and spinal cordinjuries; Disorders of the eye, such as, for example, retinitispigmentosa, blindness, color-blindness, macular degeneration.Somatostatin Inhibits growth hormone, Inhibition of growth Cancer;Metastatic carcinoid tumors; Vasoactive 2798, 2825, 2830, 2831, SeeTable 2, SEQ ID NO: Z (Octreotide; glucagons and insulin; hormonerelease in humans Intestinal Peptide secreting adenomas; Diarrhea 2902for particular construct. octreotide acetate; Suppresses LF response bysomatostatin can be and Flushing; Prostatic disorders and cancers;Sandostating to GnRH; Decreases measured as described in J. Breastcancer; Gastrointestinal disorders and LAR ®) splanchnic blood flow;Clin. Endocrinol. Metab. cancers; Cancers of the endocrine system; HeadInhibits release of (1973) October; 37(4): 632-4. and neckparagangliomas; Liver disorders and serotonin, gastrin, Inhibition ofinsulin cancers; Nasopharyngeal cancers; Thyroid vasoactive intestinalsecretion by somatostatin disorders and cancers; Acromegaly; Carcinoidpeptide, secretin, motilin, can be measured as Syndrome; Gallbladderdisorders, such as and pancreatic described in the Lancet gallbladdercontractility diseases and abnormal polypeptide. (1973) Dec. 8; bilesecretion; Psoriasis; Diabetes; Diabetes 2(7841): 1299-1301. Insipidus;Diabetes mellitus; Type 1 diabetes; Type 2 diabetes; Insulin resistance;Insulin deficiency; Hyperlipidemia; Hyperketonemia; Non-insulindependent Diabetes Mellitus (NIDDM); Insulin-dependent Diabetes Mellitus(IDDM); A Condition Associated With Diabetes Including, But Not LimitedTo Obesity, Heart Disease, Hyperglycemia, Infections, Retinopathy,And/Or Ulcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX; Kidney disorders; Neurological disorders and diseases, includingAlzheimers Disease, Parkinson's disease and dementia; Neuropsychoticdisorders, including Bipolar affective disorder; Rheumatoid arthritis;Hypertension; Intracranial hypertension; Esophageal varices; Graves'disease; Seizures; Epilepsy; Gastritis; Angiogenesis; IL-22 (IL22,Stimulates glucose uptake IL-22 activity may be Hyperglycemia; Diabetes;Diabetes Insipidus; 2901, 2903 See Table 2, SEQ ID NO: Z interleukin-22;in skeletal muscle cells; assayed in vitro using a [3- Diabetesmellitus; Type 1 diabetes; Type 2 for particular construct. IL17D, IL27)increases skeletal muscle H]-glucose uptake assay. (J diabetes; Insulinresistance; Insulin deficiency; insulin sensitivity. Biol Chem 1999 Oct.22; Hyperlipidemia; Hyperketonemia; Non-insulin 274(43): 30864-30873).dependent Diabetes Mellitus (NIDDM); Insulin- dependent DiabetesMellitus (IDDM); A Condition Associated With Diabetes Including, But NotLimited To Obesity, Heart Disease, Hyperglycemia, Infections,Retinopathy, And/Or Ulcers; Metabolic Disorders; Immune Disorders;Obesity; Vascular Disorders; Suppression of Body Weight; Suppression ofAppetite; Syndrome X. HCE1P80 Stimulates glucose uptake HCE1P80 activitymay be Hyperglycemia; Diabetes; Diabetes Insipidus; 2908, 3049, 3050,3051, See Table 2, SEQ ID NO: Z in; increases insulin assayed in vitrousing a [3- Diabetes mellitus; Type 1 diabetes; Type 2 3052 forparticular construct. sensitivity. H]-glucose uptake assay. (J diabetes;Insulin resistance; Insulin deficiency; Biol Chem 1999 Oct. 22;Hyperlipidemia; Hyperketonemia; Non-insulin 274(43): 30864-30873).dependent Diabetes Mellitus (NIDDM); Insulin- dependent DiabetesMellitus (IDDM); A Condition Associated With Diabetes Including, But NotLimited To Obesity, Heart Disease, Hyperglycemia, Infections,Retinopathy, And/Or Ulcers; Metabolic Disorders; Immune Disorders;Obesity; Vascular Disorders; Suppression of Body Weight; Suppression ofAppetite; Syndrome X. HDRMI82 Stimulates glucose HDRMI82 activity may beHyperglycemia; Diabetes; Diabetes Insipidus; 2909 See Table 2, SEQ IDNO: Z uptake; increases insulin assayed in vitro using a [3- Diabetesmellitus; Type 1 diabetes; Type 2 for particular construct. sensitivity.H]-glucose uptake assay. (J diabetes; Insulin resistance; Insulindeficiency; Biol Chem 1999 Oct. 22; Hyperlipidemia; Hyperketonemia;Non-insulin 274(43): 30864-30873). dependent Diabetes Mellitus (NIDDM);Insulin- dependent Diabetes Mellitus (IDDM); A Condition Associated WithDiabetes Including, But Not Limited To Obesity, Heart Disease,Hyperglycemia, Infections, Retinopathy, And/Or Ulcers; MetabolicDisorders; Immune Disorders; Obesity; Vascular Disorders; Suppression ofBody Weight; Suppression of Appetite; Syndrome X. HDALV07 Modulatesinsulin action Insulin activity may be Diabetes; Diabetes Insipidus;Diabetes mellitus; 3053, 3055, 3056 See Table 2, SEQ ID NO: Z(adiponectin; assayed in vitro using a [3- Type 1 diabetes; Type 2diabetes; Insulin for particular construct. gelatin-binding H] glucoseuptake assay. (J resistance; Insulin deficiency; Hyperlipidemia; 28kprotein Biol Chem 1999 Oct. 22; Hyperketonemia; Non-insulin dependentprecurson; 274(43): 30864-30873). Diabetes Mellitus (NIDDM);Insulin-dependent adipose most Diabetes Mellitus (IDDM); A Conditionabundant gene Associated With Diabetes Including, But Not transcript;APM- Limited To Obesity, Heart Disease, 1; GBP28; Hyperglycemia,Infections, Retinopathy, And/Or ACRP30; Ulcers; Metabolic Disorders;Immune Disorders; ADIPOQ) Obesity; Vascular Disorders; Suppression ofBody Weight; Suppression of Appetite; Syndrome X; Hyperglycemia;Familial combined hyperlipidemia; Metabolic syndrome; Inflammatorydisorders; Atherogenic disorders C Peptide An insulin precursorC-peptide concentrations Diabetes; Diabetes Insipidus; Diabetesmellitus; 3088, 3149 See Table 2, SEQ ID NO: Z involved in insulin canbe measured using Type 1 diabetes; Type 2 diabetes; Insulin forparticular construct. regulation assays well known in the resistance;Insulin deficiency; Hyperlipidemia; art, such as the one Hyperketonemia;Non-insulin dependent described in PNAS (1970) Diabetes Mellitus(NIDDM); Insulin-dependent September; 67(1): 148-55 Diabetes Mellitus(IDDM); A Condition Associated With Diabetes Including, But Not LimitedTo Obesity, Heart Disease, Hyperglycemia, Infections, Retinopathy,And/Or Ulcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX; Hyperglycemia; Familial combined hyperlipidemia; Metabolic syndromeHCBOG68 Controls proliferation/ Activation of cAMP- Treatment ofObesity; treatment of Diabetes; 3106, 3270 See Table 2, SEQ ID NO: Z(enteric differentiation or mediated transcription in suppression ofbody weight gain; suppression of for particular construct. adipokine;Fat metabolism/ adipocytes can be assayed appetite. Hyperglycemia;Diabetes; Diabetes SID; proline rich physiology/pathology/of usingmethods known in the Insipidus; Diabetes mellitus; Type 1 diabetes;acidic protein) adipocytes and adipose art (Berger et al., Gene 66: 1-Type 2 diabetes; Insulin resistance; Insulin tissue in response to 10(1998); Cullen and deficiency; Hyperlipidemia; Hyperketonemia; dietaryconditions. Malm, Methods in Enzymol Non-insulin dependent DiabetesMellitus 216: 362-368 (1992); (NIDDM); Insulin-dependent DiabetesMellitus Henthorn et al., Proc Natl (IDDM); A Condition Associated WithDiabetes Acad Sci USA 85: 6342- Including, But Not Limited To Obesity,Heart 6346 (1988); Reusch et al., Disease, Hyperglycemia, Infections,Retinopathy, Mol Cell Biol 20(3): 1008- And/Or Ulcers; MetabolicDisorders; Immune 1020 (2000); and Klemm et Disorders; Obesity; VascularDisorders; al., J Biol Chem 273: 917- Suppression of Body Weight;Suppression of 923 (1998)). Appetite; Syndrome X. Other indications forantibodies and/or antagonists, include treatment of weight loss;treatment of AIDS wasting; appetite stimulant; treatment of cachexia.PYY (Peptide Decreases appetite; Appetite and food intake can Mostpreferred: Treatment of Obesity; treatment 3108, 3109, 3281, 3117, SeeTable 2, SEQ ID NO: Z YY), including increases satiety; be can bemeasured by of Diabetes; suppression of body weight gain; 3118, 3282.for particular construct. PYY₃₋₃₆ decreases food intake. methods knownin the art suppression of appetite. (amino acid (Batterham et al. NatureHyperglycemia; Diabetes; Diabetes Insipidus; residues 31-64 of 2002;418: 650654) Diabetes mellitus; Type 1 diabetes; Type 2 full length PYY,diabetes; Insulin resistance; Insulin deficiency; amino acidHyperlipidemia; Hyperketonemia; Non-insulin residues 3-36 of dependentDiabetes Mellitus (NIDDM); Insulin- mature PYY) dependent DiabetesMellitus (IDDM); A Condition Associated With Diabetes Including, But NotLimited To Obesity, Heart Disease, Hyperglycemia, Infections,Retinopathy, And/Or Ulcers; Metabolic Disorders; Immune Disorders;Obesity; Vascular Disorders; Suppression of Body Weight; Suppression ofAppetite; Syndrome X. Other indications for antibodies, antagonists:treatment of weight loss; treatment of AIDS wasting; appetite stimulant;treatment of cachexia. WNT10b Inhibits adipogenesis. WNT10b activity canbe Most preferred: Treatment of Obesity; 3141 See Table 2, SEQ ID NO: Zmeasured using suppression of body weight gain; suppression of forparticular construct. adipogenesis inhibition appetite. assays (Ross etal., Science Other indications: Hyperglycemia; Diabetes; 2000;289(5481): 950-953 Diabetes Insipidus; Diabetes mellitus; Type 1diabetes; Type 2 diabetes; Insulin resistance; Insulin deficiency;Hyperlipidemia; Hyperketonemia; Non-insulin dependent Diabetes Mellitus(NIDDM); Insulin-dependent Diabetes Mellitus (IDDM). WNT11 Promotescardiogenesis. WNT11 activity can be Treatment of Cardiovasculardisorders; 3142 See Table 2, SEQ ID NO: Z measured using assaysCongestive Heart Failure; Myocardial Infarction. for particularconstruct. known in the art, including cardiogenesis assays (Eisenberget al., Dev Dyn 1999 September; 216(1): 45-58). Herstatin Inhibitscancer Herstatin activity can be Oncology; Cancer; Solid Tumors;Melanoma; 3143 See Table 2, SEQ ID NO: Z proliferation. measured usingcell Malignant Melanoma; Renal Cancer (e.g., Renal for particularconstruct. proliferation assays known Cell Carcinoma); Lung Cancer (e.g,. Non-Small in the art (Doherty et al., Cell Lung Cancer or Small CellLung Cancer); PNAS 1999; 96(19): 10869- Colon Cancer; Breast Cancer;Liver Cancer; 10874. Prostate Cancer; Bladder Cancer; Gastric Cancer;Sarcoma; AIDS-Related Kaposi's Sarcoma; Lymphoma; T Cell Lymphoma;Cutaneous T- Cell Lymphoma; Non-Hodgkin's Lymphoma; Brain Cancer;Glioma; Glioblastoma Multiforme; Cervical Dysplasia; Leukemia;Preleukemia; Hairy Cell Leukemia; Chronic Myelogeonus Leukemia;Hematological Malignancies; Hematological Disorders; Multiple Myeloma.Adrenomedullin stimulates vasodilation; Vasodilation can be Treatment ofCongestive Heart Failure; 3144 See Table 2, SEQ ID NO: Z promotes bonegrowth. measured using assays Hypertension; Myocardial Infarction;Septic for particular construct. known in the art (Ashton et Shock;Osteoporosis; Postmenopausal al. Pharmacology 2000; osteoporosis;Osteopenia. 61(2): 101-105. The promotion of bone growth can be measuredusing assays known in the art, such as the osteoblast proliferationassay (Cornish et al. Am J Physiol 1997 December; 273(6 Pt 1):E1113-20). Nogo Receptor Receptor for the axon The promotion of axonTreatment of Central Nervous System Damage; 3184, 3185 See Table 2, SEQID NO: Z growth inhibitor, Nogo. regeneration and growth can Spinal CordInjury; Peripheral Nerve Damage; for particular construct. be measuredusing assays Neurodegenerative Diseases; Parkinson's known in the art(Fournier et Disease; Alzheimer's Disease; Huntington's al. Nature 2001;Disease; Amyotrophic Lateral Sclerosis; 409(6818): 341-346). ProgressiveSupranuclear Palsy; Creutzfeld- Jacob Disease; Motor Neuron Disease.CART (Cocaine- Inhibits food intact and Appetite and food intake canMost preferred: Treatment of Obesity; 3232 See Table 2, SEQ ID NO: Z andfat storage; promotes lipid be can be measured by suppression of bodyweight gain; suppression of for particular construct. Amphetamine-oxidation. methods known in the art appetite. Regulated (Batterham etal. Nature Other indications: Hyperglycemia; Diabetes; Transcript) 2002;418: 650654) Diabetes Insipidus; Diabetes mellitus; Type 1 diabetes;Type 2 diabetes; Insulin resistance; Insulin deficiency; Hyperlipidemia;Hyperketonemia; Non-insulin dependent Diabetes Mellitus (NIDDM);Insulin-dependent Diabetes Mellitus (IDDM). RegIV (Colon Stimulatesglucose RegIV activity may be Hyperglycemia; Diabetes; DiabetesInsipidus; 2910. See Table 2, SEQ ID NO: Z Specific Gene; uptake;increases insulin assayed in vitro using a [3- Diabetes mellitus; Type 1diabetes; Type 2 for particular construct. Colon Specific sensitivity.H]-glucose uptake assay. (J diabetes; Insulin resistance; Insulindeficiency; Protein) Biol Chem 1999 Oct. 22; Hyperlipidemia;Hyperketonemia; Non-insulin 274(43): 30864-30873). dependent DiabetesMellitus (NIDDM); Insulin- dependent Diabetes Mellitus (IDDM); ACondition Associated With Diabetes Including, But Not Limited ToObesity, Heart Disease, Hyperglycemia, Infections, Retinopathy, And/OrUlcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX. Cosyntropin Synthetic corticotropin; The activity of cosyntropinEndocrine; Addison's disease; Cushing's SEQ ID: NO: 2198 (Cortrosyn)stimulates the release of can be assessed in vivo by syndrome; pituitarydysfunction; acute adrenal (CAS-16960-16- cortisol. measuring serumcortisol crisis 0) levels. (Frank et al. J. Am. Vet. Med. Assoc. 1998212(10): 1569-71). Pexiganan Disrupts bacterial Pexiganan acetateactivity Treatment of Infectious Diseases; Treatment of SEQ ID NO: 2199Acetate membranes. can be assessed using in Bacterial Infections.(CAS-172820-23- vitro antibacterial assays 4) known in the art. (Zasloffet al., Antimicrobial Agents and Chemotherapy 1999, 43: 782-788).Pramlintide Slows gastric emptying; Appetite and food intake canTreatment of Obesity; treatment of Diabetes; SEQ ID NO: 2200 (Amylin)decreases food intake. be can be measured by suppression of body weightgain; suppression of (CAS-151126-32- methods known in the art appetite;treatment of endocrine disorders; 8) (Batterham et al. NatureHyperglycemia; Diabetes; Diabetes Insipidus; 2002; 418: 650654) Diabetesmellitus; Type 1 diabetes; Type 2 diabetes; Insulin resistance; Insulindeficiency; Hyperlipidemia; Hyperketonemia; Non-insulin dependentDiabetes Mellitus (NIDDM); Insulin- dependent Diabetes Mellitus (IDDM);A Condition Associated With Diabetes Including, But Not Limited ToObesity, Heart Disease, Hyperglycemia, Infections, Retinopathy, And/OrUlcers; Metabolic Disorders; Immune Disorders; Obesity; VascularDisorders; Suppression of Body Weight; Suppression of Appetite; SyndromeX. Other indications for antibodies, antagonists: treatment of weightloss; treatment of AIDS wasting; appetite stimulant; treatment ofcachexia. Teriparatide Acts in conjuction with Adenylyl cyclase BoneDisorders; Fracture prevention; SEQ ID NO: 2201 (CAS-52232-67-calcitonin to control stimulation in rat Hypercalcemia; Malignanthypercalcemia; 4) calcium and phosphate osteosarcoma cells,Osteoporosis; Paget's disease; Osteopenia, metabolism; elevatesovariectomized rat model of Osteoclastogenesis; osteolysis;osteomyelitis; blood calcium level; osteoporosis: IUBMB Lifeosteonecrosis; periodontal bone loss; stimulates the activity of 2000February; 49(2): 131-5 osteoarthritis; rheumatoid arthritis;osteopetrosis; osteocytes; enhances periodontal, lytic, or metastaticbone disease; absorption of Ca+/Pi from osteoclast differentiationinhibition; bone small intestine into blood; disorders; bone healing andregeneration. promotes reabsorption of Ca+ and inhibits Pi by kidneytubules. Terlipressin Analog of vasopressin; Terlipressin activity canbe Variceal hemorrhage; cirrhosis; portal SEQ ID NO: 2202 (triglycyllycine induces vasoconstriction. measured using assays of hypertension;hepatorenal syndrome; Blood- vasopressin) vasoconstriction, such as therelated disorders (CAS-14636-12- isolated arterial ring 5) preparation.(Landstrom et al., Hum Reprod 1999 January; 14(1): 151-5). UlaritideStimulates natriuresis, Ularitide activity can be Excretory disorders;Acute renal failure; asthma; SEQ ID NO: 2203 (CAS-118812-69- diuresis,and vasodilation. assessed by measuring congestive heart failure;hypertension; pulmonary 4) cGMP accumulation in rat hypertension;cardiovascular disorders renal cells. (Valentin et al., Hypertension1993 April; 21(4): 432-8). Aprotinin Serine protease inhibitor;Inhibition of thrombin- Inhibition of fibrinolysis; reduction of bloodloss SEQ ID NO: 2204 (Trasylol) attenuates Systemic induced plateletaggregation during surgery; Treatment of Inflammation and(CAS-9087-70-1; Inflammatory Response, can be measured using ImmuneDisorders. CAS-11061-94-2; fibrinolysis and thrombin- methods known inthe art. CAS-12407-79-3) induced platelet (Poullis et al., J Thoracaggregation. Cardiovasc Surg 2000 August; 120(2): 370-8). AspartocinAntibacteria Aspartocin activity can be Treatment of InfectiousDiseases; treatment of SEQ ID NO: 2205 (CAS-4117-65-1; assessed using invitro bacterial infections. CAS-1402-89-7) antibacterial assays known inthe art. (Zasloff et al., Antimicrobial Agents and Chemotherapy 1999,43: 782-788). Calcitonin Regulates levels of Hypocalcemic Rat Bioassay,Musculoskeletal; Osteroporosis; Paget's disease; SEQ ID NO: 2206(Calcimar) calcium and phosphate in bone resorbing assay andhypercalcemia; (CAS-21215-62- serum; causes a reduction the pit assay,CT receptor Bone Disorders; Fracture prevention; Malignant 3) in serumcalcium--an binding assay, CAMP hypercalcemia; Osteopenia,Osteoclastogenesis; effect opposite to that of stimulation assay: J Boneosteolysis; osteomyelitis; osteonecrosis; human parathyroid Miner Res1999 periodontal bone loss; osteoarthritis; rheumatoid hormone. August;14(8): 1425-31 arthritis; osteopetrosis; periodontal, lytic, ormetastatic bone disease; osteoclast differentiation inhibition; bonedisorders; bone healing and regeneration. Carperitide Stimulatesnatriuresis, Carperitide activity can be Treatment of Heart Failure;Cardiovascular SEQ ID NO: 2207 (HANP; diuresis, and vasodilation.assessed in vitro by disorders; Respiratory disorders; Acute recombinantmeasuring cGMP respiratory distress syndrome. human atrial accumulationin a number of natriuretic cell lines, including PC12 peptide) cells andcultured human (CAS-89213-87- glomerular cells. (Medvede 6) et al., LifeSci 2001 Aug. 31; 69(15): 1783-90; Green et al., J Am Soc Nephrol 1994October; 5(4): 1091-8). Desirudin Inhibits thrombin; inhibits Desirudinactivity can be Blood-related disorder; Thrombosis; SEQ ID NO: 2208(recombinant blood clotting. assessed using blood thrombocytopenia;hemorrhages. hirudin; Revasc) clotting assays known in the(CAS-120993-53- art, such as in vitro platelet 5) aggragation assays.(Glusa, Haemostasis 1991; 21 Suppl 1: 116-20). Emoctakin proinflammatorycytokine Treatment of Inflammation, Immune disorders, SEQ ID NO: 2209(interleukin 8) RSV infection. (CAS-142298-00- 8) Felypressin Derivativeof Felypressin vasoconstriction Treatment of pain; to induce localanesthesia. SEQ ID NO: 2210 (CAS-56-59-7) Vasopressin; Stimulatesactivity can be measured vasoconstriction; Induces using assays of localanesthesia. vasoconstriction, such as the isolated arterial ringpreparation. (Landstrom et al., Hum Reprod 1999 January; 14(1): 151-5).Glucagon Induces hyperglycemia. Glucagon activity may be Hypoglycemia;Diabetes; Diabetes Insipidus; SEQ ID NO: 2211 (CAS-16941-32- assayed invitro using a [3- Diabetes mellitus; Type 1 diabetes; Type 2 5)H]-glucose uptake assay. (J diabetes; Insulin resistance; Insulindeficiency; Biol Chem 1999 Oct. 22; Hyperlipidemia; Hyperketonemia;Non-insulin 274(43): 30864-30873). dependent Diabetes Mellitus (NIDDM);Insulin- dependent Diabetes Mellitus (IDDM); A Condition Associated WithDiabetes Including, But Not Limited To Obesity, Heart Disease,Hyperglycemia, Infections, Retinopathy, And/Or Ulcers; MetabolicDisorders; Immune Disorders; Obesity; Vascular Disorders; Suppression ofBody Weight; Suppression of Appetite; Syndrome X; Endocrine disorders.Nagrestipen Inflammation; Immune SEQ ID NO: 2212 (CAS-166089-33- 4)Pentigetide Respiratory; Allergy; Immune SEQ ID NO: 2213 (Pentyde)(CAS-62087-72- 3) Proinsulin Stimulates glucose uptake Insulin activitymay be Hyperglycemia; Diabetes; Diabetes Insipidus; SEQ ID NO: 2214(CAS-67422-14- and promotes assayed in vitro using a [3- Diabetesmellitus; Type 1 diabetes; Type 2 4) glycogenesis and H]-glucose uptakeassay. (J diabetes; Insulin resistance; Insulin deficiency; lipogenesis.Biol Chem 1999 Oct. 22; Hyperlipidemia; Hyperketonemia; Non-insulin274(43): 30864-30873). dependent Diabetes Mellitus (NIDDM); Insulin-dependent Diabetes Mellitus (IDDM); A Condition Associated With DiabetesIncluding, But Not Limited To Obesity, Heart Disease, Hyperglycemia,Infections, Retinopathy, And/Or Ulcers; Metabolic Disorders; ImmuneDisorders; Obesity; Vascular Disorders; Suppression of Body Weight;Suppression of Appetite; Syndrome X. Becaplermin Promotes wound healing.Becaplermin activity can be Stimulate Epithelial Cell Proliferation;Stimulate SEQ ID NO: 2215 (Regranex; assessed using animal BasalKeratinocytes; Promote Wound Healing; recombinant wound healing modelsStimulate Hair Follicle Production; Healing Of PDGF-BB) known in theart. (Saba et Dermal Wounds. Wound Healing; Eye Tissue (CAS-165101-51-al., Ann Plast Surg 2002 Wounds, Dental Tissue Wounds, Oral Cavity 9)July; 49(1): 62-6). Wounds, Diabetic Ulcers, Dermal Ulcers, CubitusUlcers, Arterial Ulcers, Venous Stasis Ulcers, Burns Resulting From HeatExposure Or Chemicals, or Other Abnormal Wound Healing Conditions suchas Uremia, Malnutrition, Vitamin Deficiencies or ComplicationsAssociated With Systemic Treatment With Steroids, Radiation Therapy orAntineoplastic Drugs or Antimetabolites; Promote Dermal ReestablishmentSubsequent To Dermal Loss; Increase the Adherence Of Skin Grafts To AWound Bed; Stimulate Re-Epithelialization from The Wound Bed; To PromoteSkin Strength; Improve The Appearance Of Aged Skin; ProliferateHepatocytes, Lung, Breast, Pancreas, Stomach, Bladder, Small Intestine,Large Intestine; Sebocytes, Hair Follicles, Type II Pneumocytes,Mucin-Producing Goblet Cells, or Other Epithelial Cells, EndothelialCells, Keratinocytes, or Basal Keratinocytes (and Their Progenitors)Contained Within The Skin, Lung, Liver, Bladder, Eye, Salivary Glands,or Gastrointestinal Tract; Reduce The Side Effects Of Gut Toxicity ThatResult From Radiation, Chemotherapy Treatments Or Viral Infections;Cytoprotector, especially of the Small Intestine Mucosa or Bladder;Mucositis (Mouth Ulcers); Regeneration Of Skin; Full and/or PartialThickness Skin Defects, including Burns, (e.g., Repopulation Of HairFollicles, Sweat Glands, And Sebaceous Glands); Psoriasis; EpidermolysisBullosa; Blisters; Gastric and/or Doudenal Ulcers; Reduce Scarring;Inflamamatory Bowel Diseases; Crohn's Disease; Ulcerative Colitis; GutToxicity; Lung Damage; Repair Of Alveoli And/or Brochiolar Epithelium;Acute Or Chronic Lung Damage; Emphysema, ARDS; Inhalation Injuries;Hyaline Membrane Diseases; Infant Respiratory Distress Syndrome;Bronchopulmonary Displasia In Premature Infants; Fulminant LiverFailure; Cirrhosis, Liver Damage caused by Viral Hepatitis and/or ToxicSubstances; Diabetes Mellitus; Inflammation; Cancer; Digestivedisorders. Ghrelin Stimulates release of Appetite and food intake canEndocrine; loss of body weight; loss of body SEQ ID NO: 2216 (Genbankgrowth hormone from be can be measured by weight associated with canceror anorexia Accession No. anterior pituitary. methods known in the artnervosa; loss of appetite; excessive appetite; AB029434) Stimulatesappetite and (Batterham et al. Nature body weight gain; Obesity;Diabetes; reduces fat burning. 2002; 418: 650654) Acromegaly; Growthfailure; Growth hormone deficiency; Growth failure and growthretardation Prader-Willi syndrome in children 2 years or older; Growthdeficiencies; Growth failure associated with chronic renalinsufficiency; Postmenopausal osteoporosis; burns; cachexia; cancercachexia; dwarfism; metabolic disorders; obesity; renal failure;Turner's Syndrome, pediatric and adult; fibromyalgia; fracturetreatment; frailty, AIDS wasting Ghrelin -binding Inhibits growthhormone Appetite and food intake can Endocrine; Obesity; Diabetes; bodyweight gain; antibody release in response to be can be measured byexcessive appetite; loss of appetite; loss of body including Ghrelin;inhibits increase methods known in the art weight. antibody in appetite.(Batterham et al. Nature fragment, or 2002; 418: 650654) dominant-negative form of Ghrelin receptor NOGO-66 Neurodegenerative disorders;spinal cord injury; SEQ ID NO: 2217 peptide fragment neuronal injury;brain trauma; stroke; multiple (Genbank sclerosis; demyelinatingdisorders; neural activity Accession No. and neurological diseases;neural cell (e.g., NP_008939 neuron, glial cell, and schwann cell)regeneration (amino acids 62- and/or growth 101)) Gastric inhibitoryIncreases nutrient uptake Nutrient uptake and Most preferred: loss ofbody weight, AIDS SEQ ID NO: 2218 polypeptide and tryglyceridetryglyceride accumulation wasting, cachexia, loss of apetite. Other:(GIP), including accumulation in can be measured by methods Obesity;Diabetes; insulin resistance; body GIP fragments adipocytes, which leadsdesribed in Miyawaki et al., weight gain; excessive appetite. (Genbankto obesity and insulin Nat. Medicine, 2002, Vol Accession No.resistance. 8(7): 738-742. NM_004123) Gastric inhibitory Increased useof fat as Fat utilization as an energy Obesity; Diabetes; Insulinresistance; body polypeptide predominant energy source can be measuredas weight gain. antibody, or source; decreased described in Miyawaki etantibody accumulation of fat in al., Nat. Medicine, 2002, fragmentsadipocytes. Vol 8(7): 738-742. Gastric inhibitory Increased use of fatas Fat utilization as an energy Most preferred: Obesity; Diabetes; bodyweight SEQ ID NO: 2219 peptide receptor predominant energy source can bemeasured as gain; excessive appetite; insulin resistance. or receptorsource; decreased described in Miyawaki et Other: loss of body weight,AIDS wasting, loss fragments or accumulation of fat in al., Nat.Medicine, 2002, of appetite. variants including adipocytes. Vol 8(7):738-742. soluble fragments or variants (Genbank Accession NumberNM_000164) POMC Activity of POMC- Preferred: resistance to stress;anti-inflammatory SEQ ID NO: 2220 (proopiomelanocortin), derivedfragments are activity; analgesic activity; increased skin includingdiverse, and well-known pigmentation; increased protein catabolism;fragments or in the art. increased gluconeogenesis; obesity; diabetes.variants (such as, See, for example, Hadley Other: decreased proteincatabolism, decreased for example, et al., Ann NY Acad Sci skinpigmentation, Addison's disease, Cushing's alpha-melanocyte 1999 Oct.20; 885: 1-21; syndrome stimulating Dores, Prog Clin Biol Res hormone,αMSH, 1990; 342: 22-7; Blalock, gamma Ann NY Acad Sci. 1999 melanocyteOct. 20; 885: 161-72). stimulating hormone, γMSH, beta-melanocytestimulating hormone, βMSH, adrenocorticotropin, ACTH, beta- endorphin,met- enkephalin) (Genbank Accession No. NM_000930) HP 467, HP228 SeeU.S. Pat. No. See U.S. Pat. No. Resistance to stress; anti-inflammatoryactivity; SEQ ID NO: 2221 (U.S. Pat. No. 6,350,430 6,350,430 analgesicactivity; increased skin pigmentation; 6,350,430) increased proteincatabolism; increased gluconeogenesis. NDP See U.S. Pat. No. See U.S.Pat. No. Resistance to stress; anti-inflammatory activity; SEQ ID NO:2222 (U.S. Pat. No. 6,350,430 6,350,430 analgesic activity; increasedskin pigmentation; 6,350,430) increased protein catabolism; increasedgluconeogenesis. Interleukin-21 Immunomodulator; IL-21 activity can beAutoimmune disorders; Inflammatory disorders; 3298 SEQ ID NO: 2177(IL-21) inhibits interferon gamma assessed by measuring Treatment ofPsoriasis; Rheumatoid Arthritis; production by Th1 cells. interferongamma Inflammatory bowel disease. production in Th1 cells. (Wurster etal.,: J Exp Med 2002 Oct. 7; 196(7): 969-77) Interleukin-4Immunomodulator; IL-4 activity can be assessed Treatment of Psoriasis;Autoimmune disorders; 3307 SEQ ID NO: 2178 (IL-4) promotes the bymeasuring Th1/Th2 Rheumatoid Arthritis; Inflammatory boweldifferentiation of T cells cytokine responses of disease; Inflammatorydisorders. into Th2 phenotype. isolated spleen cells in vitro. (Waltz etal., Horm Metab Res 2002 October; 34(10): 561- 9). Osteoclast Inhibitsosteoclast Osteoclast Inhibitory Lectin Treatment of Bone Disorders;Osteoporosis; 3312 SEQ ID NO: 2181 Inhibitory Lectin formation. activitycan be assessed Fracture prevention; Hypercalcemia; Malignant (OCIL)using osteoclast formation hypercalcemia; Paget's disease; Osteopenia,assays known in the art. Osteoclastogenesis; osteolysis; osteomyelitis;(Zhou et al., J Biol Chem osteonecrosis; periodontal bone loss; 2002Dec. osteo arthritis; rheumatoid arthritis; osteopetrosis; 13; 277(50):48808-15) periodontal, lytic, or metastatic bone disease; osteoclastdifferentiation inhibition; bone healing and regeneration.

TABLE 2 Fusion Construct Expression SEQ ID SEQ ID SEQ ID SEQ ID SEQ IDLeader No. ID Construct Name Description Vector NO: Y NO: X NO: Z NO: ANO: B Sequence 1 1520 pC4:HSA/TR6.V30-H300 Amino acids V30 to H300 ofTR6 pC4 217 1 433 649 650 HSA (fragment shown as V1 to H271 of SEQ IDNO: 433) fused downstream of HSA. 2 1537 pYPG:HSA.TR6coV30-E294 Aminoacids V30 to E294 of TR6 pYPGaf 218 2 434 651 652 HSA (fragment shown asV1 to E265 of SEQ ID NO: 434) fused downstream of HSA. DNA encoding TR6has been codon optimized. 3 1545 pYPG:HSA.TR6coV30-L288 Amino acids V30to L288 of TR6 pYPGaf 219 3 435 653 654 HSA (fragment shown as V1 toL259 of SEQ ID NO: 435) fused downstream of HSA. DNA encoding TR6 hasbeen codon optimized. 4 1546 pYPG:HSA.TR6coV30-R284 Amino acids V30 toR284 of TR6 pYPGaf 220 4 436 655 656 HSA (fragment shown as V1 to R255of SEQ ID NO: 436) fused downstream of HSA. DNA encoding TR6 has beencodon optimized. 5 1568 pSAC35:HSA-yTR6 TR6 fused downstream of HSA. DNApSAC35 221 5 437 657 658 HSA/kex2 encoding TR6 has been codon optimized.6 1570 pSAC35:TR6-HSA Mature TR6 fused downstream of the pSAC35 222 6438 659 660 HSA/kex2 HSA/kex2 leader and upstream of the mature HSA. 71622 pC4:synTR6.M1-H300.HSA Synthetic TR6 fused upstream of mature pC4223 7 439 661 662 Native HSA, with 2 extra amino acids between TR6 theTR6 and HSA portions. 8 1623 pC4:HSA.synTR6.V30-H300 Synthetic matureTR6 fused downstream pC4 224 8 440 663 664 HSA of FL HSA. Last aminoacid HSA sequence is missing at BSU36I site. 9 1642pSAC35:GCSF.T31-P204.HSA Mature GCSF cloned downstream of the pSAC35 2259 441 665 666 HSA/kex2 HSA/kex2 leader and upstream of the mature HSA 101643 pSAC35:HSA.GCSF.T31-P204 Mature GCSF cloned downstream of thepSAC35 226 10 442 667 668 HSA/kex2 mature HSA and HSA/kex2 leadersequence. 11 1645 pSAC35:yTR6(N173Q).HSA Mutant mature TR6 clonedupstream of pSAC35 227 11 443 669 670 HSA/kex2 mature HSA and downstreamof the HSA/kex2 leader sequence. 12 1657 pC4.HSA:DeCAF.A23-D233 Aminoacids A23 to D233 of DeCAF pC4 228 12 444 671 672 HSA fused downstreamof full length HSA. 13 1680 pYPG:HSA.BLyS.A134-L285 Amino acids A134 toL285 of BLyS pYPGaf 229 13 445 673 674 HSA fused downstream of FL HSA.Two extra amino acids (Leu, Glu) have been added between the therapeuticprotein and HSA portions. 14 1681 pYPG.HSA.MPIF.D45-N120 Amino acids D45to N120 of MPIF fused pYPGaf 230 14 446 675 676 HSA downstream of FLHSA. Two additional amino acids (L and E) have been added between HSAand MPIF. 15 1697 pSAC35:HSA.GM-CSF.A18-E144 Amino acids A18 to E144 ofGM-CSF pSAC35 231 15 447 677 678 HSA fused downstream of FL HSA. 16 1699pSAC35:GM-CSF.A18-E144:HSA Amino acids A18 to E144 of GM-CSF pSAC35 23216 448 679 680 HSA/kex2 fused upstream of mature HSA and downstream ofHSA/kex2 leader. 17 1700 pSAC35:HSA-yTR6(N173Q) Mutant TR6 fuseddownstream of mature pSAC35 233 17 449 681 682 HSA/kex2 HSA withHSA/kex2 leader sequence. 18 1702 pYPG:HSA.ek.TR6coV30-L288 Amino acidsV30 to L288 of TR6 pYPGaf 234 18 450 683 684 HSA (fragment shown as V1to L259 of SEQ ID NO: 450) fused downstream of FL HSA with anenterokinase site in between. DNA encoding TR6 has been codon optimized.19 1703 pYPG:HSA.ek.TR6coV30-R284 Amino acids V30 to R284 of TR6 pYPGaf235 19 451 685 686 HSA (fragment shown as V1 to R255 of SEQ ID NO: 451)fused downstream of HSA with an enterokinase site in between. DNAencoding TR6 has been codon optimized. 20 1704 pYPG:HSA.TR6.V30-E294Amino acids V30 to E294 of TR6 fused pYPGaf 236 20 452 687 688 HSAdownstream of HSA. Two additional amino acids (Leu, Glu) are in betweenHSA and TR6. 21 1746 pYPG:HSA.ek.KDI.L28-K207 Amino acids L28 to K207 ofKDI fused pYPGaf 237 21 453 689 690 HAS downstream of HSA with anenterokinase site in between. 22 1747 pSAC35.HSA.hGHRF.Y32-L75 Aminoacids Y32 to L75 of hGHRF fused pSAC35 238 22 454 691 692 HSA downstreamof HSA. 23 1748 pSAC35.hGHRF.Y32-L75.HSA Amino acids Y32 to L75 of hGHRF(see pSAC35 239 23 455 693 694 HSA/kex2 also SEQ ID NO: 454) fusedupstream of mature HSA and downstream of HSA/kex2 leader sequence. 241749 pSAC35:HSA.PTH.S1-F3 FL HSA fused upstream of amino acids pSAC35240 24 456 695 696 HSA S1-F34 of PTH 25 1750 pSAC35:PTH.S1-F34.HSA Aminoacids 1-34 of PTH fused pSAC35 241 25 457 697 698 HSA/kex2 upstream ofmature HSA and downstream of HSA/kex2 leader sequence. 26 1757pSAC35:IL2.A21-T153.145C/S.HSA Mature human IL-2 with a single aminopSAC35 242 26 458 699 700 HSA/kex2 acid mutation (C to S at position145) cloned downstream of the HSA/KEX2 leader and upstream of mature HSA27 1758 pSAC35:HSA.IL2.A21-T153.145C/S Mature human IL-2 with a singleamino pSAC35 243 27 459 701 702 HSA/kex2 acid mutation (C to S atposition 145) cloned downstream of HSA with HSA/kex2 leader sequence. 281772 pSAC:EPOco.A28-D192.HSA Amino acids A28-D192 of EPO variant pSAC35244 28 460 703 704 HSA/kex2 (where glycine at amino acid 140 has beenreplaced with an arginine) fused upstream of mature HSA and downstreamof HSA/kex2 leader sequence. DNA encoding EPO has been codon optimized.29 1774 pSAC:HSA.EPOco.A28-D192. Amino acids A28-D192 of EPO variantpSAC35 245 29 461 705 706 HSA/kex2 (where glycine at amino acid 140 hasbeen replaced with an arginine) fused downstream of HSA with HSA/kex2leader sequence. DNA encoding EPO has been codon optimized. 30 1777pSAC35:TNFR2.L23-D257.HSA Mature TNFR2 fused downstream of the pSAC35246 30 462 707 708 HSA/kex2 HSA/kex2 signal and upstream of mature HSA.31 1778 pSAC35:IFNβ.M22-N187:HSA Residues M22-N187 of full-length IFNbpSAC35 247 31 463 709 710 HSA/kex2 (shown as M1 to N166 of SEQ ID NO:463) fused upstream of mature HSA and downstream of HSA/kex2 leadersequence. 32 1779 pSAC35:HSA:IFNβ.M22-N187 Residues M22-N187 offull-length IFNb pSAC35 248 32 464 HSA/kex2 (shown as M1 to N166 of SEQID NO: 464) fused downstream of HSA with HSA/kex2 leader sequence. 331781 pSAC:EPOcoA28-D192.HSA Amino acids A28-D192 of EPO variant pSAC35249 33 465 711 712 HSA/kex2 51N/S, 65N/S, 110N/s (where glycine at aminoacid 140 has been replaced with an arginine) fused upstream of matureHSA and downstream of HSA/kex2 leader sequence. Glycosylation sites atamino acid 51, 65, 110 are mutated from N to S residue. DNA encoding EPOhas been codon optimized. 34 1783 pSAC:HSA.EPOcoA28-D192.51N/S, Aminoacids A28-D192 of EPO variant pSAC35 250 34 466 713 714 HSA/kex2 65N/S,110N/s (where glycine at amino acid 140 has been replaced with anarginine) fused downstream of HSA with HSA/kex2 leader sequence.Glycosylation sites at amino acids 51, 65, 110 are mutated from N to Sresidue. DNA encoding EPO has been codon optimized. 35 1784pSAC35:HSA.TNFR2.L23-D257 Mature TNFR2 fused downstream of FL pSAC35 25135 467 715 716 HSA HSA. 36 1785 pSAC35:KGF2A28.Δ63-S208:HSA Amino acidsA63 to S208 of KGF2 fused pSAC35 252 36 468 717 718 HSA/kex2 upstream ofmature HSA and downstream of the HSA/kex2 signal peptide. 37 1786pSAC35:HSA.KGF2{D}28.A63-S208 Amino acids A63 to S208 of KGF2 fusedpSAC35 253 37 469 719 720 HSA downstream of HSA. 38 1788pSAC35:HSA.TR2.P37-A192 Amino acids P37 to A192 of TR2 fused pSAC35 25438 470 721 722 HSA/kex2 downstream of HSA with HSA/kex2 leader sequence.39 1793 pSAC35:HSA.EPO.A28-D192 Amino acids A28-D192 of EPO variantpSAC35 255 39 471 HSA/kex2 (N51A, N65A, N110A) (where glycine at aminoacid 140 has been replaced with an arginine; see, for example, SEQ IDNO: 499) fused downstream of HSA with HSA/kex2 leader sequence.Glycosylation sites at amino acids 51, 65, 110 are mutated from N to Aresidue. 40 1794 pSAC35:HSA.EPO.A28-D192 Amino acids A28-D192 of the EPOpSAC35 256 40 472 HSA/kex2 variant (where glycine at amino acid 140 hasbeen replaced with an arginine; see, for example, SEQ ID NO: 499) fuseddownstream of HSA with HSA/kex2 leader sequence. 41 1809pSAC35.MDC.G25-Q93.HSA Amino acids P26 to Q93 of MDC with an pSAC35 25741 473 723 724 HSA/kex2 N-terminal methionine, fused downstream of theHSA/kex2 leader and upstream of mature HSA. 42 1812pSAC35:IL2.A21-T153.HSA Amino acids A21 to T153 of IL-2 fused pSAC35 25842 474 725 726 HSA/kex2 downstream of the HSA/kex2 leader and upstreamof mature HSA. 43 1813 pSAC35:HSA.IL2.A21-T153 Amino acids A21 to T153of IL-2 fused pSAC35 259 43 475 727 728 HSA/kex2 downstream of HSA withHSA/kex2 leader sequence. 44 1821 pSAC35:scFv116A01.HSA BLyS antibodyfused upstream of mature pSAC35 260 44 476 729 730 Modified HSA whichlacks the first 8 amino acids HSA/kex2, and downstream from the HSA/kex2lacking the signal sequence which lacks the last two last two aminoacids. amino acids 45 1830 pSAC35:HSA.KEX2.HAGDG59.L19-Q300 Amino acidsL19-Q300 of HAGDG59 pSAC35 261 45 477 731 732 HSA/kex2 fused downstreamof the HSA/kex2 signal, mature HSA and KEX2 cleavage site. 46 1831pSAC35:HAGDG59.L19-Q300.HSA HSA/kex2 signal peptide followed by pSAC35262 46 478 733 734 HSA/kex2 amino acids L19-Q300 of HAGDG59 followed bymature HSA. 47 1833 pSAC35:humancalcitonin.C1-G33:HSA Human Calcitonin(amino acids C98- pSAC35 263 47 479 735 736 HSA/kex2 G130 of SEQ ID NO:479) fused upstream of mature HSA and downstream of HSA/kex2 leadersequence. 48 1834 pSAC35:HSA.humancalcitonin.C1-G33 Human Calcitonin(amino acids C98- pSAC35 264 48 480 737 738 HSA G130 of SEQ ID NO: 480)fused downstream of FL HSA. 49 1835 pSAC35:salmoncalcitonin.C1-G33:HSASalmon Calcitonin amino acids C1-G33 pSAC35 265 49 481 739 740 HSA/kex2fused upstream of mature HSA and downstream of HSA/kex2 leader sequence.50 1836 pSAC35:HSA.salmoncalcitonin.C1-G33 Salmon Calcitonin amino acidsC1-G33 pSAC35 266 50 482 741 742 HSA fused downstream of HSA. 51 1853pSAC35:PTH(1-34)N26.HSA Amino acids 1 to 34 of PTH fused pSAC35 267 51483 743 744 HSA/kex2 upstream of mature HSA and downstream of HSA/kex2leader sequence. Amino acid K26 of PTH mutated to N26. 52 1854pSAC35:HSA.PTH(l-34)N26 Amino acids 1 to 34 of PTH fused pSAC35 268 52484 745 746 HSA downstream of HSA. Amino acid K26 of PTH mutated to N26.53 1862 pSAC35:HSA.GnRH.Q24-G33 Amino acids Q24-G33 of human pSAC35 26953 485 747 748 HSA/kex2 gonadotropin releasing hormone fused downstreamof HSA with HSA/kex2 leader sequence. 54 1863 pSAC35:GnRHQ24-G33.HSAAmino acids Q24-G33 of human pSAC35 270 54 486 749 750 HSA/kex2gonadotropin releasing hormone fused upstream of mature HSA anddownstream of HSA/kex2 leader sequence. 55 1866 pSAC35:teprotide.HSATeprotide fused upstream of mature HSA. pSAC35 271 55 487 751 752 561867 pSAC35:HSA.teprotide. Teprotide fused downstream of FL HSA. pSAC35272 56 488 753 754 HSA 57 1889 pC4:HSA.PTH.S1-F34 PTH(l-34) fuseddownstream of HSA. pC4 273 57 489 755 756 HSA 58 1891 pEE12:HSA.sTR6Soluble mature TR6 fused downstream of pEE12.1 274 58 490 757 758 HSAHSA. 59 1892 pEE12:sTR6.HSA Synthetic full length TR6 fused upstreampEE12.1 275 59 491 759 760 TR6 of mature HSA. 60 1906 pC4:PTH.S1-F34.HSAAmino acids S1 to F34 of PTH fused pC4 276 60 492 761 762 MPIF(junctioned) upstream of mature HSA and downstream of MPIF leadersequence. There are two cloning junction amino acids (T, S) between PTHand HSA. 61 1907 pC4:HSA.PTH.S1-F34 Amino acids S1 to F34 fuseddownstream pC4 277 61 493 763 764 HSA (junctioned) of FL HSA. The lastC-terminal amino acid (L) residue is missing for HSA in the cloningjunction between HSA and PTH. 62 1912 pC4:sTR6.HSA Synthetic full lengthTR6 fused upstream pC4 278 62 494 765 766 Native of mature HSA. TR6leader 63 1913 pC4:HSA.synTR6.V30-H300 (seamless) Amino acids V30 toH300 of synthetic pC4 279 63 495 767 768 HSA TR6 (shown as V1 to H271 ofSEQ ID NO: 495) fused downstream of full-length HSA. 64 1914pC4:PTH.S1-F34.HSA Amino acids S1 to F34 of PTH fused pC4 280 64 496 769770 MPIF (seamless) downstream of MPIF leader sequence and upstream ofmature HSA. 65 1916 pC4:HSA.KGF2D28.A63-S208 Amino acids A63 to S208 offull length pC4 281 65 497 771 772 HSA KGF2 fused downstream of HSA. 661917 pC4:KGF2D28.A63-S208:HSA Amino acids A63 to S208 of KGF2 fused pC4282 66 498 773 774 HSA/kex2 upstream of mature HSA. 67 1925 pcDNA3.EPOM1-D192.HSA Amino acids M1 to D192 of EPO variant pcDNA3 283 67 499 775776 Native (where glycine at amino acid 140 has EPO leader been replacedwith an arginine) fused peptide upstream of HSA. D192 of EPO and D1 ofmature HSA are the same amino acids in this construct. 68 1926pcDNA3:SPHSA.EPO Amino acids A28 to D192 of EPO variant pcDNA3 284 68500 777 778 MPIF A28-D192 (where glycine at amino acid 140 has beenreplaced with an arginine) fused upstream of mature HSA and downstreamof the MPIF leader peptide. 69 1932 pEE12.1:HSA.PTH.S1-F34 Amino acids 1to 34 of PTH fused pEE12.1 285 69 501 779 780 HSA downstream of fulllength HSA. 70 1933 pSAC35:HCC-l.T20-N93:HSA Amino acids T20 to N93 ofHCC-1 fused pSAC35 286 70 502 781 782 HSA/kex2 upstream of mature HSAand downstream of the HSA/kex2 leader sequence. 71 1934pSAC35:HCC-1C.O.T20-N93:HSA Amino acids T20 to N93 of HCC-1 fused pSAC35287 71 503 783 784 HSA/kex2 upstream of mature HSA and downstream of theHSA/kex2 leader sequence. DNA sequence is codon optimized for yeastexpression. 72 1938 pEE12.1:PTH.S1-F34.HSA Amino acids S1 to F34 of PTHfused pEE12.1 288 72 504 785 786 MPIF upstream of mature HSA anddownstream of MPIF leader sequence. 73 1941 pC4:HSA/PTH84 PTH fuseddownstream of full length pC4 289 73 505 787 788 HSA (junctioned) HSA.The last amino acid of HSA (Leu) has been deleted. 74 1947pSAC35:d8HCC-l.G28-N93:HSA Amino acids G28 to N93 of HCC-1 fused pSAC35290 74 506 789 790 HSA/kex2 upstream of mature HSA and downstream ofHSA/kex2 leader sequence. 75 1948 pSAC35:d8HCC-1C.O.G28-N93:HSA Aminoacids G28 to N93 of HCC-1 fused pSAC35 291 75 507 791 792 HSA/kex2upstream of mature HSA and downstream of HSA/kex2 leader sequence. DNAsequence is codon optimized for yeast expression. 76 1949pC4:PTH.S1-Q84/HSA PTH fused downstream of the MPIF pC4 292 76 508 793794 MPIF (junctioned) leader sequence and upstream of mature HSA. Thereare two additional amino acids between PTH84 and HSA as a result of thecloning site. 77 1952 pcDNA3.1:IL2.HSA Full length human IL-2, having apCDNA3.1 293 77 509 795 796 Native IL- Cysteine to Serine mutation atamino acid 2 leader 145, fused upstream of mature HSA. 78 1954pC4:IL2.HSA Full length human IL-2, having a pC4 294 78 510 797 798Native IL- Cysteine to Serine mutation at amino acid 2 leader 145, fusedupstream of mature HSA. 79 1955 pSAC35:t9HCC-l.G28-N93:spcHSA Aminoacids G28 to N93 of HCC-1 fused pSAC35 295 79 511 799 800 HSA/kex2upstream of a 16 amino acid spacer and mature HSA and downstream ofHSA/kex2 leader sequence. 80 1956 pSAC35:HSA.scFv116A01 Single chainBLyS antibody fused pSAC35 296 80 512 801 802 HSA/kex2 downstream of HSAwith HSA/kex2 leader sequence. This construct also contains a His tag atthe 3′ end. 81 1966 pC4:EPO.M1-D192.HSA Amino acids M1 to D192 of EPOvariant pC4 297 81 513 Native Construct is also named (where glycine atamino acid 140 has EPO leader pC4:EPOM1-D192.HSA been replaced with anarginine) fused peptide upstream of mature HSA. 82 1969pC4:MPIFsp.HSA.EPO.A28-D192 Amino acids A28 to D192 of EPO variant pC4298 82 514 MPIF (where glycine at amino acid 140 has been replaced withan arginine) fused downstream of MPIF leader sequence and upstream ofmature HSA. 83 1980 pC4:EPO.A28-D192.HSA Amino acids A28 to D192 of EPOvariant pC4 299 83 515 803 804 HSA (where glycine at amino acid 140 hasbeen replaced with an arginine) fused downstream of the HSA leaderpeptide and upstream of mature HSA. 84 1981 pC4.HSA-EPO.A28-D192. Aminoacids A28 to D192 of EPO variant pC4 300 84 516 805 806 HSA (whereglycine at amino acid 140 has been replaced with an arginine) fuseddownstream of the full length HSA. 85 1989 pSACS5:activeAC2inhibitor:HSAActive inhibitor of ACE2 (DX512) fused pSAC35 301 85 517 807 808HSA/kex2 upstream of mature HSA and downstream of HSA/kex2 leadersequence. 86 1994 pEE12.1.HSA-EPO.A28-D192. Amino acids A28 to D192 ofEPO variant pEE12.1 302 86 518 HSA (where glycine at amino acid 140 hasbeen replaced with an arginine) fused downstream of full length HSA. 871995 pEE12.1:EPO.A28-D192. HSA Amino acids A28 to D192 of EPO variantpEE12.1 303 87 519 HSA (where glycine at amino acid 140 has beenreplaced with an arginine) fused downstream of the HSA leader peptideand upstream of mature HSA. 88 1996 pEE12.1:MPIFsp.HSA.EPO.A28-D192Amino acids A28 to D192 of EPO variant pEE12.1 304 88 520 MPIF (whereglycine at amino acid 140 has been replaced with an arginine) fuseddownstream of MPIF leader sequence and upstream of mature HSA. 89 1997pEE12.1:EPO M1-D192.HSA Amino acids M1 to D192 of EPO variant pEE12.1305 89 521 Native (where glycine at amino acid 140 has EPO leader beenreplaced with an arginine) fused upstream of mature HSA. 90 1998pC4:CKB1.G28-N93.HSA Amino acids G28 to N93 of CkBeta1 pC4 306 90 522809 810 HSA fused upstream of mature HSA and downstream of the HSAleader sequence. 91 2000 pSAC35:HSA:activeAC2inhibitor Active inhibitorof ACE2 (DX512) fused pSAC35 307 91 523 811 812 HSA downstream of HSA.92 2001 pSAC35:inactiveAC2inhibitor:HSA Inactive inhibitor of ACE2(DX510) pSAC35 308 92 524 813 814 HSA/kex2 fused upstream of mature HSAand downstream of HSA/kex2 leader sequence. 93 2002pSAC35:HSA.inactiveAC2inhibitor Inactive inhibitor of ACE2 (DX510)pSAC35 309 93 525 815 816 HSA fused downstream of HSA. 94 2011pC4:IFNb-HSA Full length IFNb fused upstream of pC4 310 94 526 817 818Native mature HSA. IFNb leader 95 2013 pC4:HSA-IFNb.M22-N187 Amino acidsM22 to N187 of IFNb pC4 311 95 527 HSA (fragment shown as amino acids M1to N166 of SEQ ID NO: 527) fused downstream of HSA. 96 2016pC4:TR1.M1-L401.HSA Amino acids M1 to L401 of TR1 fused pC4 312 96 528819 820 Native upstream of mature HSA. Native TR1 TR1 signal sequenceused. A Kozak sequence was added. 97 2017 pC4:HSA.TR1.E22-L401 Aminoacids E22 to L401 of TR1 fused pC4 313 97 529 821 822 HSA downstream ofHSA. 98 2021 pC4:PTH.S1-Q84/HSA Amino acids 1-84 of PTH fused upstreampC4 314 98 530 823 824 HSA (seamless) of mature HSA and downstream ofnative HSA leader sequence. 99 2022 pEE12.1:PTH.S1-Q84.HSA Amino acids1-84 of PTH fused upstream pEE12.1 315 99 531 HSA of mature HSA anddownstream of native HSA leader sequence. 100 2023 pSAC35.PTH.S1-Q84.HSAAmino acids 1-84 of PTH fused upstream pSAC35 316 100 532 825 826HSA/kex2 of mature HSA and downstream of HSA/kex2 leader sequence. 1012025 pSAC35:teprotide.spacer.HSA Teprotide fused upstream of a linkerand pSAC35 317 101 533 827 828 mature HSA. 102 2026pSAC35:HSA.spacer.teprotide Teprotide fused downstream of HSA and pSAC35318 102 534 829 830 HSA a linker. 103 2030 pSAC35.ycoIL-2.A21-T153.HSAAmino acids A21 to T153 of IL-2 fused pSAC35 319 103 535 831 832HSA/kex2 upstream of mature HSA and downstream of HSA/kex2 leadersequence. DNA encoding IL-2 has been codon optimized. 104 2031pSAC35.HSA.ycoIL-2.A21-T153 Amino acids A21 to T153 of IL-2 fused pSAC35320 104 536 833 834 HSA/kex2 downstream of HSA with the HSA/kex2 leadersequence. DNA encoding IL-2 has been codon optimized. 105 2047pC4HSA:SP.EPO A28-D192.HSA Amino acids A28 to D192 of EPO variant pSAC35321 105 537 835 836 MPIF (where glycine at amino acid 140 has beenreplaced with an arginine) fused upstream of mature HSA and downstreamof MPIF leader peptide. 106 2053 pEE12:IFNb-HSA Full length IFNb fusedupstream of pEE12.1 322 106 538 Native also named mature HSA. IFNbpEE12.1:IFNβ-HSA leader 107 2054 pEE12:HSA-IFNb Mature IFNb fuseddownstream of HSA. pEE12.1 323 107 539 HSA 108 2066pC4:GM-CSF.M1-E144.HSA Amino acids M1 to E144 of GM-CSF pC4 324 108 540837 838 Native fused upstream of mature HSA. GM-CSF 109 2067pC4:HSA.GM-CSF.A18-E144 Amino acids A18 to E144 of GM-CSF pC4 325 109541 839 840 HSA fused downstream of HSA. 110 2085pEE12.1:TR1.M1-L401.HSA Amino acids M1 to L401 of TR1 fused pEE12.1 326110 542 Native upstream of mature HSA. TR-1 111 2086pEE12.1:HSA.TR1.E22-L401 Amino acids E22 to L401 (fragment pEE12.1 327111 543 HSA shown as amino acids E1 to L380 of SEQ ID NO: 543) of TR1fused downstream of HSA. 112 2095 pC4:HSA-BLyS.A134 Amino acids A134 toL285 of BLyS pC4 328 112 544 841 842 HSA fused downstream of HSA. 1132096 pC4:sp.BLyS.A134-L285.HSA Amino acids A134 to L285 of BLyS pC4 329113 545 843 844 Native (fragment shown as amino acids A1 to CKβ8 L152 ofSEQ ID NO: 545) fused upstream of mature HSA and downstream of the CKb8signal peptide. 114 2101 pcDNA3:SP.Ck7 Q22-A89.HSA. N-terminalMethionine fused to amino pcDNA3 330 114 546 845 846 MPIF acids Q22 toA89 of Ckβ7 fused upstream of mature HSA and downstream of MPIF signalpeptide. 115 2102 pEE12.1:SP.EPO A28-D192.HSA Amino acids A28 to D192 ofEPO variant pEE12.1 331 115 547 MPIF (where glycine at amino acid 140has been replaced with an arginine) fused upstream of mature HSA anddownstream of MPIF leader peptide. 116 2129 pC4:TR2.M1-A192.HSA Aminoacids M1-A192 of TR2 fused pC4 332 116 548 847 848 Native upstream ofHSA. TR2 117 2137 pSAC35.MDC.G25-Q93.HSA. Amino acids G25 to Q93 of MDCfused pSAC35 333 117 549 849 850 HSA/kex2 upstream of mature HSA anddownstream of HSA/kex2 leader sequence. 118 2141 HSA-CK-Beta4 Fulllength CK-beta4 fused downstream pSAC35 334 118 550 851 852 HSA of HSA.119 2146 pC4:Leptin.HSA Full length Leptin fused upstream of pC4 335 119551 853 854 Native mature HSA. leptin 120 2181 pC4:HSA.IL1Ra(R8-E159)Amino acids R8 to E159 of IL1Ra (plus pC4 336 120 552 855 856 HSA anadded methionine at N-terminus) fused downstream of HSA. 121 2182pC4:MPIFsp(M1-A21).IL1Ra(R8-E159).HSA Amino acids R8 to E159 of IL1Ra(plus pC4 337 121 553 857 858 MPIF an added methionine at N-terminus)fused downstream of the MPIF leader sequence and upstream of mature HSA.122 2183 pSAC35:HSA.IL1Ra(R8-E159) Amino acids R8 to E159 of IL1Ra (pluspSAC35 338 122 554 859 860 HSA an added methionine at N-terminus) fuseddownstream of HSA. 123 2184 pC4:HSA.Leptin.V22-C166 Amino acids V22 toC167 of Leptin fused pC4 339 123 555 861 862 HSA downstream of HSA. 1242185 pSAC35:IL1Ra(R8-E159).HSA Amino acids R8 to E159 of IL1Ra (pluspSAC35 340 124 556 863 864 HSA/kex2 an added methionine at N-terminus)fused upstream of mature HSA and downstream of HSA/kex2 leader sequence.125 2186 pSAC35:Leptin.V22-C166.HSA Amino acids V22 to C167 of Leptinfused pSAC35 341 125 557 865 866 HSA/kex2 upstream of mature HSA anddownstream of HSA/kex2 leader sequence. 126 2187pSAC35:HSA.Leptin.V22-C166 Amino acids V22 to C167 of Leptin pSAC35 342126 558 867 868 HSA/kex2 fused downstream of HSA with HSA/kex2 leadersequence. 127 2226 pcDNA3(+):TREM-1(21-202)-HSA Amino acids A21 to P202of TREM-1 pCDNA3.1 343 127 559 869 870 MPIF fused upstream of mature HSAand downstream of the MPIF leader sequence. 128 2230pC4:TREM-1.M1-P202.HSA Amino acids M1 to P202 of TREM-1 pC4 344 128 560871 872 Native fused upstream of mature HSA. TREM-1 129 2240 pC4:SP.Ck7Q22-A89.HSA. N-terminal Methionine fused to amino pC4 345 129 561 873874 MPIF acids Q22 to A89 of Ckβ7 fused upstream of mature HSA anddownstream of the MPIF leader sequence. Contains a linker sequencebetween Ckβ7 and HSA. 130 2241 pC4:HSA.Ck7metQ22-A89. N-terminalMethionine fused to amino pC4 346 130 562 875 876 HSA/kex2 acids Q22 toA89 of Chemokine beta 7 (Ckbeta 7 or CK7) fused downstream of HSA withHSA/kex2 leader sequence. Contains a linker sequence between CkB7 andHSA. 131 2244 pC4.HCNCA73.HSA HCNCA73 fused upstream of mature pC4 347131 563 877 878 HCNCA73 HSA. 132 2245 pScNHSA:CK7.Q22-A89 Amino acidsQ22 to A89 of Ckβ7 fused pScNHSA 348 132 564 879 880 HSA/kex2 downstreamof HSA with HSA/kex2 leader sequence. Contains a linker sequence betweenCkβ7 and HSA. 133 2246 pScCHSA.CK7metQ22-A89 N-terminal Methionine fusedto amino pScCHSA 349 133 565 881 882 HSA/kex2 acids Q22 to A89 of Ckβ7fused upstream of mature HSA and downstream of HSA/kex2 leader sequence.134 2247 pSAC35:CK7metQ22-A89.HSA. N-terminal Methionine fused to aminopSAC35 350 134 566 883 884 HSA/kex2 acids Q22 to A89 of Ckβ7 fusedupstream of mature HSA and downstream of HSA/kex2 leader sequence. 1352248 pSAC35:HSA.CK7metQ22-A89. N-terminal Methionine fused to aminopSAC35 351 135 567 885 886 HSA/kex2 acids Q22 to A89 of Ckβ7 fuseddownstream of HSA with HSA/kex2 leader sequence. Contains a linkersequence between Ckβ7 and HSA. 136 2249 pSAC35:IFNa2-HSA Mature IFNa2fused upstream of mature pSAC35 352 136 568 887 888 HSA/kex2 also named:HSA and downstream of HSA/kex2 pSAC23:IFNα2-HSA leader sequence. 1372250 pSAC35:HSA.INSULIN(GYG) Mature Insulin wherein the C-peptide ispSAC35 353 137 569 889 890 HSA also named: replaced by the C-domain ofIGF-1 fused pSAC35.HSA.INSULING(GYG).F1-N62 downstream of HSA. DNAencoding Insulin was codon optimized. 138 2251 pScCHSA:VEGF2.T103-R227.Amino acids T103 to R227 of VEGF2 pScCHSA 354 138 570 891 892 HSA/kex2fused upstream of mature HSA and downstream of HSA/kex2 leader sequence.139 2252 pScNHSA:VEGF2.T103-R227. Amino acids T103 to R227 of VEGF2pScNHSA 355 139 571 893 894 HSA/kex2 fused downstream of HSA withHSA/kex2 leader sequence. 140 2255 pSAC35:INSULIN(GYG).HSA MatureInsulin wherein the C-peptide is pSAC35 356 140 572 895 896 HSA/kex2also named replaced by the C-domain of IGF-1 fusedpSAC35.INSULING(GYG).F1-N62.HSA upstream of mature HSA and downstream ofHSA/kex2 leader. DNA encoding Insulin was codon optimized. 141 2256pSAC35:VEGF2.T103-R227.HSA Amino acids T103 to R227 of VEGF2 pSAC35 357141 573 897 898 HSA/kex2 fused upstream of mature HSA and downstream ofHSA/kex2 leader sequence. 142 2257 pSAC35:HSA.VEGF2.T103-R227 Aminoacids T103 to R227 of VEGF-2 pSAC35 358 142 574 899 900 HSA/kex2 fuseddownstream of HSA with HSA/kex2 leader sequence. 143 2271pEE12.1:HCHNF25M1-R104.HSA Amino acids M1 to R104 of HCHNF25 pEE12.1 359143 575 Native fused upstream of mature HSA. HCHNF25 144 2276pSAC35:HSA.INSULIN(GGG) Mature Insulin wherein the C-peptide is pSAC35360 144 576 901 902 HSA also named: replaced by a synthetic linker fusedpSAC35.HSA.INSULIN G(GGG).F1-N58 downstream of HSA. DNA encoding Insulinwas codon optimized. 145 2278 pSAC35:insulin(GGG).HSA Mature Insulinwherein the C-peptide is pSAC35 361 145 577 903 904 HSA/kex2 replaced bya synthetic linker fused downstream of HSA/kex2 leader and upstream ofmature HSA. DNA encoding Insulin was codon optimized. 146 2280pC4:HCHNF25.HSA HCHNF25 fused upstream of mature pC4 362 146 578 905 906Native HSA. HCHNF25 147 2283 pScCHSA:EPOcoA28-D192.51N/Q, Amino acidsA28 to D192 of EPO variant pScCHSA 363 147 579 907 908 HSA/kex2 65N/Q,110N/Q EPO (where glycine at amino acid 140 has been replaced with anarginine) are fused upstream of mature HSA and downstream of HSA/kex2leader sequence. Glycosylation sites at amino acids 51, 65 and 110 aremutated from N to Q residue. DNA encoding EPO is codon optimized. 1482284 pScNHSA:EPOcoA28-D192.51N/Q, Amino acids A28 to D192 of EPO variantpScNHSA 364 148 580 909 910 HSA/kex2 65N/Q, 110N/Q EPO (where glycine atamino acid 140 has been replaced with an arginine) fused downstream ofmature HSA and HSA/kex2 leader sequence. Glycosylation sites at aminoacids 51, 65 and 110 are mutated from N to Q residue. DNA encoding EPOis codon optimized. 149 2287 pSAC35:EPOcoA28-D192.51N/Q, Amino acids A28to D192 of EPO variant pSAC35 365 149 581 911 912 HSA/kex2 65N/Q,110N/Q.HSA. (where glycine at amino acid 140 has been replaced with anarginine) fused upstream of mature HSA and downstream of HSA/kex2 leadersequence. Glycosylation sites at amino acid 51, 65 and 110 are mutatedfrom N to Q residue. DNA encoding EPO is codon optimized. 150 2289pSAC35:HSA.EPOcoA28-D192.51N/Q, Amino acids A28 to D192 of EPO variantpSAC35 366 150 582 913 914 HSA/kex2 65N/Q, 110N/Q. (where glycine atamino acid 140 has been replaced with an arginine) fused downstream ofmature HSA and HSA/kex2 leader sequence. Glycosylation sites at aminoacid 51, 65 and 110 are mutated from N to Q residue. DNA encoding EPO iscodon optimized. 151 2294 pC4:EPO.R140G.HSA Amino acids M1-D192 of EPOfused pC4 367 151 587 915 916 Native also named upstream of mature HSA.The EPO EPO pC4.EPO.R1406.HSA sequence included in construct 1997 wasused to generate this construct, mutating arginine at EPO amino acid 140to glycine. This mutated sequence matches the wildtype EPO sequence. 1522295 pSAC35:humanresistin.K19-P108:HSA Amino acids K19 to P108 ofResistin pSAC35 368 152 584 917 918 HSA/kex2 fused upstream of matureHSA and downstream of HSA/kex2 leader sequence. 153 2296pSAC35:HSA:humanresistin.K19-P108 Amino acids K19 to P108 of ResistinpSAC35 369 153 585 919 920 HSA fused downstream of HSA. 154 2297pSAC35:humanresistin.K19-P108.stop:HSA Amino acids K19 to P108 ofResistin pSAC35 370 154 586 921 922 HSA/kex2 fused upstream of matureHSA and downstream of HSA/kex2 leader sequence. Includes two stops at 3′end for termination of translation before the HSA. 155 2298pEE12.1:EPO.R140G.HSA Amino acids M1 to D192 of EPO fused pEE12.1 371155 587 923 924 Native upstream of mature HSA. The EPO EPO sequenceincluded in construct 1997 was used to generate this construct, mutatingarginine at EPO amino acid 140 to glycine. This mutated sequence matchesthe wildtype EPO sequence. 156 2300 pC4:humanresistin.M1-P108:HSA Aminoacids M1 to P108 of Resistin pC4 372 156 588 925 926 Native fusedupstream of mature HSA. resistin 157 2309pEE12.1:humanresistin.M1-P108:HSA Amino acids M1 to P108 of ResistinpEE12.1 373 157 589 927 Native fused upstream of mature HSA. resistin158 2310 pc4:EPOco.M1-D192.HSA Amino acids M1 to D192 of EPO variant pC4374 158 590 928 929 Native fused upstream of mature HSA. DNA EPOencoding EPO is codon optimized. The EPO sequence included in construct1997 was used to generate this construct, mutating arginine at EPO aminoacid 140 to glycine. This mutated sequence matches the wildtype EPOsequence. 159 2311 pC4:EPO.M1-G27.EPOco.A28-D192.HSA Amino acids M1 toD192 of EPO fused pC4 375 159 591 930 931 Native upstream of mature HSA.DNA encoding EPO only EPO portion is codon optimized. The EPO sequenceincluded in construct 1997 was used to generate this construct, mutatingarginine at EPO amino acid 140 to glycine. This mutated sequence matchesthe wildtype EPO sequence. 160 2320 pC4:HCHNF25M1-R104.HSA Amino acidsM1 to R104 of HCHNF25 pC4 376 160 592 932 933 Native fused upstream ofmature HSA. HCHNF25 161 2325 pC4.EPO:M1-D192.HSA.Codon opt. Amino acidsM1 to D192 of EPO fused pC4 377 161 593 Native upstream of mature HSA.DNA encoding EPO EPO is codon optimized. 162 2326pEE12.1.EPO:M1-D192.HSA.Codon opt. Amino acids M1 to D192 of EPO fusedpEE12.1 378 162 594 Native upstream of mature HSA. DNA encoding EPO EPOis codon optimized. 163 2328 pC4:HLDOU18.K23-R429.HSA Amino acids K23 toR429 of HLDOU18 pC4 379 163 595 934 935 HSA fused upstream of mature HSAand downstream of native HSA leader sequence. 164 2330 CK-Beta4-HSA Fulllength Ckbeta4 fused upstream of pSAC35 380 164 596 936 937 Nativemature HSA. CKβ4 165 2335 pC4:MPIFsp.ck{b}4D31-M96.HSA Amino acids D31to M96 of Ckbeta4 pC4 381 165 597 938 939 MPIF fused upstream of matureHSA and downstream of MPIF leader sequence. 166 2336pC4:MPIFsp.ck{b}4G35-M96.HSA Amino acids G35 to M96 of Ckbeta4 pC4 382166 598 940 941 MPIF fused upstream of mature HSA and downstream of MPIFleader sequence. 167 2337 pC4:MPIFsp.ck{b}4G48-M96.HSA Amino acids G48to M96 of Ckbeta4 pC4 383 167 599 942 943 MPIF fused upstream of matureHSA and downstream of MPIF leader sequence. 168 2338pC4:MPIFsp.ck{b}4A62-M96.HSA Amino acids A62 to M96 of Ckbeta4 pC4 384168 600 944 945 MPIF fused upstream of mature HSA and downstream of MPIFleader sequence. 169 2340 pC4:HSA.HLDOU18.K23-R429 Amino acids K23 toR429 of HLDOU18 pC4 385 169 601 946 947 HSA fused downstream of HSA. 1702343 pSAC35.INV-IFNA2.HSA Mature Interferon alpha2 fused upstream pSAC35386 170 602 948 949 invertase of mature HSA and downstream of invertasesignal peptide. 171 2344 pC4.SpIg.EPO:A28-D192.HSA.Codon opt. Aminoacids A28 to D192 of EPO fused pC4 387 171 603 950 951 Mouse Ig upstreamof mature HSA and downstream leader of mouse Ig leader sequence. DNAencoding EPO is codon optimized. 172 2348 pC4:MPIFsp.ck{b}4G57-M96.HSAAmino acids G57 to M96 of Ckbeta4 pC4 388 172 604 952 953 MPIF fusedupstream of mature HSA and downstream of MPIF leader sequence. 173 2350pC4:MPIFsp.HLDOU18(S320-R429).HSA Amino acids S320 to R429 of HLDOU18pC4 389 173 605 954 955 MPIF fused upstream of mature HSA and downstreamof MPIF leader sequence. 174 2351 pC4:HSA.HLDOU18(S320-R429) Amino acidsS320 to R429 of HLDOU18 pC4 390 174 606 956 957 HSA fused downstream ofHSA. 175 2355 pSAC35:MATalpha.d8ckbeta1.G28-N93:HSA Amino acids G28 toN93 of Ckbeta1 pSAC35 391 175 607 958 959 MFα-1 fused upstream of matureHSA and downstream of the yeast mating factor alpha leader sequence. 1762359 pEE12:HLDOU18.K23-R429.HSA Amino acids K23 to R429 of HLDOU18pEE12.1 392 176 608 HSA fused upstream of mature HSA and downstream ofnative HSA leader sequence. 177 2361 pC4:HRDFD27:HSA HRDFD27 fusedupstream of mature HSA. pC4 393 177 609 960 961 Native HRDFD27 178 2362pEE12:HSA.HLDOU18.K23-R429 Amino acids K23 to R429 of HLDOU18 pEE12.1394 178 610 HSA fused downstream of HSA. 179 2363pC4GCSF.HSA.EPO.A28-D192 Amino acids M1 to P204 of GCSF fused pC4 395179 611 Native upstream of mature HSA which is fused GCSF upstream ofamino acids A28 to D192 of EPO variant (where amino acid 140 of EPO ismutated from glycine to arginine.) 180 2365 pEE12.1.HCNCA73HSA HCNCA73is fused upstream of mature pEE12.1 396 180 612 962 963 Native HSA.HCNCA73 181 2366 pSAC35.MAF-IFNa2.HSA Mature IFNa2 fused upstream ofmature PSAC35 397 181 613 964 965 MFα-1 HSA and downstream of yeastmating factor alpha leader sequence. 182 2367pEE12.MPIFsp.HLDOU18.S320-R429.HSA Amino acids S320 to R429 of HLDOU18pEE12.1 398 182 614 966 967 MPIF fused upstream of mature HSA anddownstream of MPIF leader sequence. 183 2369 pC4:HLDOU18.HSA Amino acidsM1 to R429 of HLDOU18 pC4 399 183 615 968 969 Native fused upstream ofmature HSA. HLDOU18 184 2370 pEE12:HLDOU18.HSA Amino acids M1 to R429 ofHLDOU18 pEE12.1 400 184 616 Native fused upstream of mature HSA. HLDOU18185 2373 pC4.GCSF.HSA.EPO.A28-D192.R140G Amino acids M1 to P204 of GCSFis pC4 401 185 617 Native fused upstream of mature HSA which is GCSFfused upstream of amino acids A28 to D192 of EPO, wherein amino acid 140is glycine. The EPO sequence included in construct 1997 was used togenerate this construct, mutating arginine at EPO amino acid 140 toglycine. This mutated sequence matches the wildtype EPO sequence. 1862381 pC4:HSA-IFNa2(C17-E181) Amino acids C17 to E181 of IFNa2 pC4 402186 618 970 971 HSA (fragment shown as amino acids C1 to E165 of SEQ IDNO: 618) fused downstream of HSA. 187 2382 pC4:IFNa2-HSA IFNa2 fusedupstream of mature HSA. pC4 403 187 619 972 973 Native IFNα2 leader 1882387 pC4:EPO(G140)-HSA-GCSF.T31-P204 Amino acids M1-D192 of EPO fusedpC4 404 188 620 Native upstream of mature HSA which is fused EPOupstream of amino acids T31 to P204 of GCSF. 189 2407pC4:HWHGZ51.M1-N323.HSA Amino acids M1 to N323 of HWHGZ51 pC4 405 189621 974 975 Native fused upstream of mature HSA. HWHGZ51 190 2408pEE12.1:HWHGZ51.M1-N323.HSA Amino acids M1 to N323 of HWHGZ51 pEE12.1406 190 622 976 977 Native fused upstream of mature HSA. HWHGZ51 1912410 pSAC35INV:IFNa-HSA Mature IFNa2 fused downstream of the pSAC35 407191 623 978 979 invertase invertase signal peptide and upstream ofmature HSA. 192 2412 pSAC35:delKEX.d8ckbeta1.G28-N93:HSA Amino acids G28to N93 of Ckbeta1 pSAC35 408 192 624 980 981 HSA fused downstream of theHSA signal minus the sequence (with the KEX site deleted - KEX site last6 amino acids of the leader) and upstream of mature HSA. 193 2414pC4.EPO:M1-D192copt.HSA.GCSF.T31-P204 Amino acids M1 to D192 of EPOfused pC4 409 193 625 982 983 Native also named: upstream of mature HSAwhich is fused EPO pC4.EPO:M1-D192copt.HAS.GCSF.T31-P204 upstream ofamino acids T31 to P204 of GCSF. DNA encoding EPO has been codonoptimized. 194 2428 pN4:PTH.S1-Q84/HSA Amino acids S1 to Q84 of PTHfused pN4 410 194 626 HSA upstream of mature HSA and downstream of thenative HSA leader sequence. 195 2441pEE12.EPO:M1-D192copt.HSA.GCSF.T31-P204 Amino acids M1 to D192 of EPOfused pEE12.1 409 196 628 EPO leader also named: upstream of mature HSAwhich is fused pEE12.EPO:M1-D192copt.HAS.GCSF.T31-P204 upstream of aminoacids T31 to P204 of GCSF. DNA encoding EPO has been codon optimized.196 2447 pC4:HSA.humancalcitonin.C1-G33 Amino acids C98 to G130 of SEQID pC4 413 197 629 986 987 HSA NO: 629 fused downstream of HSA. 197 2448pSAC35:GLP-1(7-36).HSA Amino acids H98 to R127 of pSAC35 414 198 630 988989 HSA/kex2 preproglucagon (SEQ ID NO: 630) (hereinafter this specificdomain will be referred to as “GLP-1(7-36)”) is fused upstream of matureHSA and downstream of HSA/kex2 leader sequence. 198 2449pSAC35:INV.d8CKB1.G28-N93:HSA Amino acids G28 to N93 of Ckbeta1 pSAC35415 199 631 990 991 Invertase fused downstream of the invertase signalpeptide and upstream of mature HSA. 199 2455 pSAC35:HSA.GLP-1(7-36)GLP-1(7-36) is fused downstream of pSAC35 416 200 632 992 993 HSA/kex2mature HSA and HSA/kex2 leader sequence. 200 2456pSAC35:GLP-1(7-36(A8G)).HSA Amino acids H98 to R127 of pSAC35 417 201633 994 995 HSA/kex2 Preproglucagon (SEQ ID NO: 633)(also referred to as“GLP-1(7-36)”) is mutated at amino acid 99 of SEQ ID NO: 633 to replacethe alanine with a glycine. This particular GLP-1 mutant will behereinafter referred to as “GLP-1(7- 36(A8G))” and corresponds to thesequence shown in SEQ ID NO: 1808. GLP-1(7-36(A8G)) is fused upstream ofmature HSA and downstream of HSA/kex2 leader sequence. 201 2457pSAC35:HSA.GLP-1(7-36(A8G)) GLP-1(7-36(A8G)) (SEQ ID NO: 1808) is pSAC35418 202 634 996 997 HSA/kex2 fused downstream of mature HSA and HSA/kex2leader sequence. 202 2469 pSAC35:HSA.exendin.H48-S86 Amino acids H48 toS86 of Extendin pSAC35 419 203 635 HSA fused downstream of full lengthHSA. 203 2470 pSAC35:Exendin.H48-S86.HSA Amino acids H48 to S86 ofExtendin pSAC35 420 204 636 HSA/kex2 fused upstream of mature HSA anddownstream of HSA/kex2 leader sequence. 204 2473pC4.HLDOU18:HSA:S320-R429 M1-R319 of HLDOU18 (containing the pC4 421 205637 998 999 Native furin site RRKR) followed by residues HLDOU18 ‘LE’followed by mature HSA followed by ‘LE’ and amino acids S320 throughR429 of HLDOU18 (fragment shown as SEQ ID NO: 637). 205 2474pSAC35.MDC.P26-Q93.HSA Amino acids P26 to Q93 of MDC fused pSAC35 422206 638 1000 1001 HSA/kex2 downstream of the HSA/kex2 leader andupstream of mature HSA. 206 2475 pSAC35.MDC.M26-Q93.HSA Amino acids Y27to Q93 of MDC with an pSAC35 423 207 639 1002 1003 HSA/kex2 N-terminalmethionine, fused downstream of the HSA/kex2 leader and upstream ofmature HSA. 207 2476 pSAC35.MDC.Y27-Q93.HSA Amino acids Y27 to Q93 ofMDC fused pSAC35 424 208 640 1004 1005 HSA/kex2 downstream of theHSA/kex2 leader and upstream of mature HSA. 208 2477pSAC35.MDC.M27-Q93.HSA Amino acids G28 to Q93 of MDC with an pSAC35 425209 641 1006 1007 HSA/kex2 N-terminal methionine, fused downstream ofthe HSA/kex2 leader and upstream of mature HSA. 209 2489pSAC35:HSA.C17.A20-R136 Amino acids A20 to R136 of C17 fused pSAC35 426210 642 1008 1009 HSA/kex2 downstream of mature HSA with HSA/kex2 leadersequence. 210 2490 pSAC35:C17.A20-R136.HSA Amino acids A20 to R136 ofC17 fused pSAC35 427 211 643 1010 1011 HSA/kex2 downstream of theHSA/kex2 leader and upstream of mature HSA. 211 2492pC4.IFNb(deltaM22).HSA Mutant full length INFbeta fused pC4 428 212 644Native upstream of mature HSA. First residue of IFNβ native, matureIFNbeta (M22) has been leader deleted. 212 2498 pC4:HSA.KGF2D60.G96-S208Amino acids G96 to S208 of KGF-2 pC4 429 213 645 1012 1013 HSA fuseddownstream of HSA. 213 2499 pC4:KGF2D60.G96-S208:HSA Amino acids G96 toS208 of KGF2 fused pC4 430 214 646 1014 1015 HSA upstream of mature HSAand downstream of the HSA signal peptide. 214 2501pSAC35:scFvI006D08.HSA BLyS antibody fused upstream of mature pSAC35 431215 647 1016 1017 HSA/kex2 HSA and downstream of HSA/kex2 signalpeptide. 215 2502 pSAC35:scFvI050B11.HSA BLyS antibody fused upstream ofmature pSAC35 432 216 648 1018 1019 HSA/kex2 HSA and downstream ofHSA/kex2 leader sequence. 216 2513 pC4:HSA.salmoncalcitonin.C1-G33 C1through G33 of salmon calcitonin pC4 1513 1345 1681 1854 1855 HSA fuseddownstream of full length HSA. 217 2515 pC4:HDPBQ71.M1-N565.HSA M1through N565 of HDPBQ71 fused pC4 1514 1346 1682 1856 1857 Nativeupstream of mature HSA HDPBQ71 218 2529 pC4:TR1.M1-K194.HSA Amino acidsM1 to K194 of TR1 pC4 1223 1208 1238 1253 1254 Native (including nativesignal sequence) fused TR1 upstream of mature HSA. 219 2530pC4:TR1.M1-Q193.HSA Amino acids M1 to Q193 of TR1 pC4 1224 1209 12391255 1256 Native (including native signal sequence) fused TR1 upstreamof mature HSA. 220 2531 pC4:TR1.M1-E203.HSA Amino acids M1 to E203 ofTR1 pC4 1225 1210 1240 1257 1258 Native (including native signalsequence) fused TR1 upstream of mature HSA. 221 2532 pC4:TR1.M1-Q339.HSAAmino acids M1 to Q339 of TR1 pC4 1226 1211 1241 1259 1260 Native(including native signal sequence) fused TR1 upstream of mature HSA. 2222545 pEE12.1:HDPBQ71.M1-N565.HSA M1 through N565 of HDPBQ71 fusedpEE12.1 1515 1347 1683 Native upstream of mature HSA HDPBQ71 223 2552pSAC35:KGF2delta33.S69-S208.HSA Amino acids S69 through S208 of KGF2pScCHSA 1516 1348 1684 1858 1859 HSA/kex2 fused upstream of HSA. 2242553 pSAC35:HSA.KGF2delta33.S69-S208 HSA/kex2 signal peptide followed bypScNHSA 1517 1349 1685 1860 1861 HSA/kex2 HSA peptide followed by aminoacids S69 to S208 of KGF2. 225 2555 pEE12.1:TR1.M1-Q193.HSA Amino acidsM1 to Q193 of TR1 pEE12.1 1227 1212 1242 Native (including native signalsequence) fused TR1 upstream of mature HSA. 226 2556pEE12.1:TR1.M1-K194.HSA Amino acids M1 to K194 of TR1 pEE12.1 1228 12131243 Native (including native signal sequence) fused TR1 upstream ofmature HSA. 227 2557 pEE12.1:TR1.M1-E203.HSA Amino acids M1 to E203 ofTR1 pEE12.1 1229 1214 1244 Native (including native signal sequence)fused TR1 upstream of mature HSA. 228 2558 pEE12.1:TR1.M1-Q339.HSA Aminoacids M1 to Q339 of TR1 pEE12.1 1230 1215 1245 Native (including nativesignal sequence) fused TR1 upstream of mature HSA. 229 2571pC4.OSCAR.R232.HSA M1-R232 of OSCAR fused upstream of pC4 1518 1350 16861862 1863 Native mature HSA. OSCAR receptor leader 230 2580pC4.IFNb(deltaM22, C38S).HSA IFNb fused upstream of mature HSA. The pC41519 1351 1687 Native IFNb used in this fusion lacks the first IFNβresidue of the mature form of IFNb, which corresponds to M22 of SEQ IDNO: 1687. Also amino acid 38 of SEQ ID NO: 1687 has been mutated fromCys to Ser. 231 2584 pC4:MPIFsp.KGF2delta28.A63-S208.HSA MPIF signalsequence followed by A63 pC4 1520 1352 1688 1864 1865 MPIF through S208of KGF2 followed by mature HSA. 232 2603 pC4:HSA(A14)-EPO(A28-D192.G140)Modified HSA A14 leader fused pC4 1521 1353 1689 Modified upstream ofmature HSA which is fused HSA (A14) upstream of A28 through D192 of EPO.Amino acid 140 of EPO is a ‘G’. 233 2604 pC4:HSA(S14)-EPO(A28-D192.G140)Modified HSA S14 leader fused upstream pC4 1522 1354 1690 Modified ofmature HSA which is fused upstream HSA (S14) of A28 through D192 of EPO.Amino acid 140 of EPO is a ‘G’. 234 2605 pC4:HSA(G14)-EPO(A28-D192.G140)Modified HSA G14 leader fused pC4 1523 1355 1691 Modified upstream ofmature HSA which is fused HSA (G14) upstream of A28 through D192 of EPO.Amino acid 140 of EPO is a ‘G’. 235 2606 pC4:HSA#64.KGF2D28.A63-S208 A63through S208 of KGF2 fused pC4 1524 1356 1692 1866 1867 Modifieddownstream of mature HSA and the HSA #64 modified #64 leader sequence.236 2607 pC4:HSA#65.KGF2D28.A63-S208 A63 through S208 of KGF2 downstreampC4 1525 1357 1693 1868 1869 Modified of mature HSA and the modified #65HSA #65 leader sequence. 237 2608 pC4:HSA#66.KGF2D28.A63-S208 A63through S208 of KGF2 fused pC4 1526 1358 1694 1870 1871 Modifieddownstream of mature HSA and the HSA #66 modified #66 leader sequence.238 2623 pC4:(AGVSG, 14-18)HSA.HLDOU18.K23-R429 A modified HSA A14leader followed by pC4 1527 1359 1695 Modified mature HSA and aminoacids K23 HSA (A14) through R429 of HLDOU18. leader 239 2624 pC4:(SGVSG,14-18)HSA.HLDOU18.K23-R429 Modified HSA S14 leader followed by pC4 15281360 1696 Modified mature HSA and amino acids K23 to HSA (S14) R429 ofHLDOU18. leader 240 2625 pC4:(GGVSG, 14-18)HSA.HLDOU18.K23-R429 Amodified HSA G14 leader sequence pC4 1529 1361 1697 Modified followed bymature HSA and amino acids HSA (G14) K23 through R429 of HLDOU18. leader241 2630 pC4:HSA.KGF2D28.A63-S208#2 Amino acids A63 to S208 of KGF-2 pC41530 1362 1698 1872 1873 HSA fused to the C-terminus of HSA. 242 2631pEE12.1:(AGVSG, 14- A modified HSA A14 leader sequence pEE12.1 1531 13631699 Modified 18)HSA.HLDOU18.K23-R429 followed by mature HSA and aminoacids HSA (A14) K23 through R429 of HLDOU18. leader 243 2632pEE12.1:(SGVSG, 14- Modified HSA S14 leader followed by pEE12.1 15321364 1700 Modified 18)HSA.HLDOU18.K23-R429 mature HSA and amino acidsK23 to HSA (S14) R429 of HLDOU18. leader 244 2633 pEE12.1:(GGVSG, 14- Amodified HSA G14 leader sequence pEE12.1 1533 1365 1701 Modified18)HSA.HLDOU18.K23-R429 followed by mature HSA and amino acids HSA (G14)K23 through R429 of HLDOU18. leader 245 2637 pSAC35:HSA.GCSF.T31-P207HSA/kex2 leader fused upstream of pScNHSA 1534 1366 1702 1874 1875HSA/kex2 mature HSA followed by T31 through P207 of GCSF (SEQ ID NO:1702). 246 2638 pPPC007:116A01.HSA scFv I116A01 with C-terminal HSApPPC007 1535 1367 1703 1876 1877 scFvI006A01 fusion, where the matureform of HSA lacks the first 8 amino acids. 247 2647 pSAC35:T7.HSA. TheT7 peptide (SEQ ID NO: 1704) of pScCHSA 1536 1368 1704 1878 1879HSA/kex2 Tumstatin was fused with a C-terminal HSA and N terminalHSA/kex2 leader. 248 2648 pSAC35:T8.HSA The T8 peptide (SEQ ID NO: 1705)of pScCHSA 1537 1369 1705 1880 1881 HSA/kex2 Tumstatin is fused upstreamto mature HSA and downstream from HSA/kex2. 249 2649 pSAC35:HSA.T7 TheT7 peptide (SEQ ID NO: 1706) of pScNHSA 1538 1370 1706 1882 1883HSA/kex2 Tumstatin was fused with a N-terminal HSA/kex2 signal sequence.250 2650 pSAC35:HSA.T8 The T8 peptide (SEQ ID NO: 1767) of pScNHSA 15391371 1707 1884 1885 HSA/kex2 Tumstatin is fused downstream to HSA/kex2signal sequence and mature HSA. 251 2656 pSac35:Insulin(KR.GGG.KR).HSASynthetic gene coding for a single-chain pScCHSA 1540 1372 1708 18861887 HSA/kex2 insulin with HSA at C-terminus. Contains a modified loopfor processing resulting in correctly disulfide bonded insulin coupledto HSA. 252 2667 pSAC35:HSA.T1249 T1249 fused downstream of full lengthpSAC35 1178 1179 1180 1181 1182 HSA HSA 253 2668pSac35:HSA.Insulin(KR.GGG.KR) Synthetic gene coding for insulin with FLpScNHSA 1541 1373 1709 1888 1889 HSA HSA at N-terminus. Contains amodified loop for processing resulting in correctly disulfide bondedinsulin coupled to HSA. 254 2669 pSac35:Insulin(GGG.KK).HSA Syntheticgene coding for a single-chain pScCHSA 1542 1374 1710 1890 1891 HSA/kex2insulin with HSA at C-terminus. Contains a modified loop. 255 2670pSAC35:T1249.HSA T1249 fused downstream of HSA/kex2 pSAC35 1183 11791180 1184 1185 HSA/kex2 leader and upstream of mature HSA. 256 2671pSac35:HSA.Insulin(GGG.KK) Synthetic gene coding for a single-chainpScNHSA 1543 1375 1711 1892 1893 HSA insulin with HSA at N-terminus.Contains a modified loop for greater stability. 257 2672 pSAC35:HSA.T20Amino terminus of T20 (codon pSAC35 1186 1187 1188 1189 1190 HSAoptimized) fused downstream of full length HSA 258 2673 pSAC35:T20.HSAAmino terminus of T20 (codon optimized) fused pSAC35 1191 1187 1188 11921193 HSA/kex2 downstream of HSA/kex2 leader and upstream of mature HSA.259 2700 pSAC35:HSA.GCSF.T31-R199 C-terminal deletion of GCSF fusedpSAC35 1544 1376 1712 1894 1895 HSA/kex2 downstream of mature HSA. 2602701 pSAC35:HSA.GCSF.T31-H200 C-terminal deletion of GCSF fused pScNHSA1545 1377 1713 1896 1897 HSA/kex2 downstream of mature HSA. 261 2702pSAC35:HSA.GCSF.T31-L201 HSA/kex2 leader followed by mature pSAC35 11941195 1196 1197 1198 HSA/kex2 HSA and amino acids T31-L201 of GCSF(corresponding to amino acids T1 to L171 of SEQ ID NO: 1196). 262 2703pSAC35:HSA.GCSF.A36-P204 HSA/kex2 leader followed by mature pScNHSA 15461378 1714 1898 1899 HSA/kex2 HSA and amino acids A36-P204 of GCSF. 2632714 pC4:HSASP.PTH34(2)/HSA PTH34 double tandem repeats fused pC4 11991200 1201 1202 1203 HSA downstream of HSA leader (with the leader KEXsite deleted - last 6 amino acids of minus Kex the leader) and upstreamof mature HSA. site 264 2724 pSAC35.sCNTF.HSA HSA/Kex2 fused to CNTF,and then pSAC35 1547 1379 1715 1900 1901 HSA/kex2 fused to mature HSA.265 2725 pSAC35:HSA.sCNTF HSA/Kex2 fused to mature HSA and pSAC35 15481380 1716 1902 1903 HSA/kex2 then to CNTF 266 2726pSac35.INV.GYGinsulin.HSA Synthetic gene coding for a single-chainpSAC35 1549 1381 1717 1904 1905 Invertase insulin with HSA atC-terminus. The signal peptide of invertase is used for this construct.267 2727 pSac35.INV.GYGinsulin(delF1).HSA Synthetic gene coding for asingle-chain pSAC35 1550 1382 1718 1906 1907 invertase insulin with HSAat C-terminus. Construct uses the invertase signal peptide and islacking the first amino acid (F) of mature human insulin. 268 2749pEE12.1.OSCAR.R232.HSA Amino acids M1 through R232 of pEE12.1 1551 13831719 1908 1909 Native OSCAR fused upstream of mature HSA. OSCAR leader269 2784 pSAC35:Insulin(GYG)-HSA codon optimized Synthetic gene codingfor a single-chain pSAC35 1552 1384 1720 1910 1911 invertase insulinwith HSA at C-terminus. 270 2789 pSAC35:Insulin(GGG).HSA (codonoptimized) Synthetic gene coding for a single-chain pSAC35 1553 13851721 1912 1913 invertase insulin with HSA at C-terminus. 271 2791pEE12.1:HSAsp.PTH34(2X).HSA Parathyroid hormone is fused in tandempEE12.1 1554 1386 1722 HSA and upstream of mature HSA and leaderdownstream from HSA signal peptide minus Kex (with the KEX sitedeleted - last 6 amino site acids of the leader) 272 2795pC4:HSA(A14)-IFNb.M22-N187 The mature form of IFNb is fused to the pC41555 1387 1723 Modified C-terminus of HSA, which contains an HSA (A14)modified signal peptide, designed to improve processing and homogeneity.273 2796 pC4:HSA(S14)-IFNb.M22-N187 The mature form of IFNb is fused tothe pC4 1556 1388 1724 Modified C-terminus of HSA, which contains a HSA(S14) modified signal peptide, designed to improve processing andhomogeneity. 274 2797 pC4:HSA(G14)-IFNb.M22-N187 The mature form of IFNbis fused to the pC4 1557 1389 1725 Modified C-terminus of HSA, whichcontains an HSA (G14) modified signal peptide. 275 2798pSAC35:Somatostatin(S14).HSA A 14 amino acid peptide of SomatostatinpScCHSA 1558 1390 1726 1914 1915 HSA/kex2 fused downstream of HSA/kex2leader and upstream of mature HSA. 276 2802pSAC35:GLP-1(7-36(A8G)).IP2.HSA GLP-1(7-36(A8G)) (SEQ ID NO: 1808) ispScNHSA 1559 1391 1727 HSA/kex2 fused downstream from the HSA/kex2leader sequence and upstream from the intervening peptide-2 ofproglucagon peptide and upstream from mature HSA. 277 2803pSAC35:GLP-1(7-36(A8G))x2.HSA GLP-1(7-36(A8G)) (SEQ ID NO: 1808) ispScCHSA 1231 1216 1246 1261 1262 HSA/kex2 tandemly repeated and fuseddownstream of the HSA/kex2 signal sequence, and upstream of mature HSA.278 2804 pSAC35:coGLP-1(7-36(A8G))x2.HSA GLP-1(7-36(A8G)) (SEQ ID NO:1808) is pScCHSA 1232 1217 1247 1263 1264 HSA/kex2 tandemly repeated andfused downstream of the HSA/kex2 signal sequence, and upstream of matureHSA. 279 2806 pC4:HSA#65.salmoncalcitonin.C1-G33 Modified HSA leader #65followed by pC4 1560 1392 1728 1916 1917 Modified mature HSA and C1-G33of salmon HSA #65 calcitonin. 280 2821 pSac35.delKex2.Insulin(GYG).HSASynthetic gene coding for a single-chain pScCHSA 1561 1393 1729 Modifiedinsulin with HSA at C-terminus. The HSA/kex2, kex2 site has been deletedfrom the lacking the HSA/KEX2 signal peptide. Kex2 site. 281 2822pSac35.alphaMF.Insulin(GYG).HSA Synthetic gene coding for a single-chainpSAC35 1562 1394 1730 1920 1921 MFα-1 insulin with HSA at C-terminus.The signal peptide of alpha mating factor (MFα-1) is used for thisconstruct. 282 2825 pSAC35:HSA.Somatostatin(S14) 14 amino acid peptideof Somatostatin pScNHSA 1563 1395 1731 1922 1923 HSA/kex2 was fuseddownstream of HSA/kex2 leader and mature HSA. 283 2830 pSAC35:S28.HSA 28amino acids of somatostatin fused pScCHSA 1564 1396 1732 1924 1925HSA/kex2 downstream of HSA/kex2 leader and upstream of mature HSA. 2842831 pSAC35:HSA.S28 28 amino acids of somatostatin fused pScNHSA 15651397 1733 1926 1927 HSA/kex2 downstream of HSA/kex2 leader and matureHSA. 285 2832 pSAC35:Insulin.HSA Long-acting insulin peptide fusedpScCHSA 1566 1398 1734 1928 1929 invertase (yeast codon optimized)upstream of mature HSA. 286 2837 pSAC35:CKB1.K21-N93:HSA K21-N93 of CKB1(fragment shown as pScCHSA 1567 1399 1735 1930 1931 HSA/kex2 K2 to N74of SEQ ID NO: 1735) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 287 2838 pSAC35:CKB1.T22-N93:HSA T22-N93 of CKB1(fragment shown as pScCHSA 1568 1400 1736 1932 1933 HSA/kex2 T3 to N74of SEQ ID NO: 1736) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 288 2839 pSAC35:CKB1.E23-N93:HSA E23-N93 of CKB1(fragment shown as pScCHSA 1569 1401 1737 1934 1935 HSA/kex2 E4 to N74of SEQ ID NO: 1737) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 289 2840 pSAC35:CKB1.S24-N93:HSA S24-N93 of CKB1(fragment shown as pScCHSA 1570 1402 1738 1936 1937 HSA/kex2 S5 to N74of SEQ ID NO: 1738) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 290 2841 pSAC35:CKB1.S25-N93:HSA S25-N93 of CKB1(fragment shown as pScCHSA 1571 1403 1739 1938 1939 HSA/kex2 S6 to N74of SEQ ID NO: 1739) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 291 2842 pSAC35:CKB1.S26-N93:HSA S26-N93 of CKB1(fragment shown as pScCHSA 1572 1404 1740 1940 1941 HSA/kex2 S7 to N74of SEQ ID NO: 1740) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 292 2843 pSAC35:CKB1.R27-N93:HSA R27-N93 of CKB1(fragment shown as pScCHSA 1573 1405 1741 1942 1943 HSA/kex2 R8 to N74of SEQ ID NO: 1741) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 293 2844 pSAC35:CKB1.P29-N93:HSA P29-N93 of CKB1(fragment shown as pScCHSA 1574 1406 1742 1944 1945 HSA/kex2 P10 to N74of SEQ ID NO: 1742) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 294 2845 pSAC35:CKB1.Y30-N93:HSA Y30-N93 of CKB1(fragment shown as pScCHSA 1575 1407 1743 1946 1947 HSA/kex2 Y11 to N74of SEQ ID NO: 1743) fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 295 2849 pC4.MPIFsp.CKB1.G28-N93.HSA G28-N93 of CKB1(fragment shown as pC4 1576 1408 1744 1948 1949 MPIF G9 to N74 of SEQ IDNO: 1744) fused downstream of the MPIF signal peptide and upstream ofmature HSA. 296 2872 pSAC35:HSA.IFNaA(C1-Q91)/D(L93-E166) This constructcontains a hybrid form of pSAC35 1309 1310 1311 1312 1313 HSA/kex2 IFNaAand IFNaD fused downstream of mature HSA. 297 2873pSAC35:HSA.IFNaA(C1-Q91)/B(L93-E166) This construct contains a hybridform of pSAC35 1314 1315 1316 1317 1318 HSA/kex2 IFNaA and IFNaB fuseddownstream of mature HSA. 298 2874 pSAC35:HSA.IFNaA(C1-Q91)/F(L93-E166)This construct contains a hybrid form of pSAC35 1319 1320 1321 1322 1323HSA/kex2 IFNaA and IFNaF fused downstream of mature HSA. 299 2875pSAC35:HSA.IFNaA(C1Q-62)/D(Q64-E166) This construct contains a hybridform of pSAC35 1324 1325 1326 1327 1328 HSA/kex2 IFNaA and IFNaD fuseddownstream of mature HSA. 300 2876 pSAC35:HSA.IFNaA(C1-Q91)/D(L93-E166);This construct contains a hybrid form of pSAC35 1329 1330 1331 1332 1333HSA/kex2 R23K, A113V IFNaA and IFNaD fused downstream of mature HSA. 3012877 pSAC35:KT.Insulin.HSA Killer toxin signal peptide fused to pScCHSA1577 1409 1745 1950 1951 Killer toxin synthetic gene coding for asingle-chain insulin with C-terminal HSA 302 2878 pSAC35:AP.Insulin.HSAAcid phospatase signal peptide fused to pSAC35 1578 1410 1746 Acidsynthetic gene coding for a single-chain phosphatase insulin withC-terminal HSA. 303 2882 pSac35.alphaMFprepro.Insulin(GYG).HSA MFα-1prepro signal followed by GYG pSAC35 1579 1411 1747 MFα-1 insulinfollowed by mature HSA. 304 2885pSac35.alphaMFpreproEEA.Insulin(GYG).HSA Yeast MFα-1 prepro signalfollowed by pSAC35 1580 1412 1748 Yeast GYG insulin follwed by matureHSA. MFα-1 305 2886 pSAC35:HSA.GCSF.P40-P204 HSA/kex2 signal peptidefollowed by pSAC35 1581 1413 1749 1952 1953 HSA/kex2 mature HSA followedby GCSF (P40- P204). 306 2887 pSAC35:HSA.GCSF.P40-L201 HSA/kex2 signalpeptide followed by pSAC35 1582 1414 1750 1954 1955 HSA/kex2 mature HSAfollowed by GCSF (P40- L201). 307 2888 pSAC35:HSA.GCSF.Q41-L201 HSA/kex2signal peptide followed by pSAC35 1583 1415 1751 1956 1957 HSA/kex2mature HSA followed by GCSF (Q41- L201). 308 2889pSAC35:HSA.GCSF.Q41-P204 HSA/kex2 signal peptide followed by pSAC35 15841416 1752 1958 1959 HSA/kex2 mature HSA followed by GCSF (Q41- P204).309 2890 pC4.HSA.GCSF.T31-P204 HSA/kex2 signal peptide followed by pC41585 1417 1753 1960 1961 HSA/kex2 mature HSA followed by GCSF (T31-P204). 310 2891 pGAP.alphaMF.Insulin(GYG).HSA Synthetic gene coding fora single-chain pYPGaf 1586 1418 1754 1962 1963 HSA/kex2 insulin with HSAat C-terminus. The signal peptide of HSA/kex2 is used for thisconstruct. 311 2897 pGAP.Insulin(KR.GGG.KR).HSA Long-acting insulinanalog using a pYPGaf 1587 1419 1755 1964 1965 HSA/kex2 synthetic genecoding for a single-chain insulin with HSA at C-terminus. Contains amodified loop for processing resulting in correctly disulfide bondedinsulin coupled to HSA 312 2900 pSAC:GLP-1(7-36)x2.HSA GLP-1(7-36) istandemly repeated and pScCHSA 1233 1218 1248 1265 1266 HSA/kex2 thenfused downstream of the HSA/kex2 signal sequence and upstream of matureHSA. 313 2901 pSAC35:IL22.A18-P202.HSA Amino acids A18-P202 of IL22fused pSAC35 1588 1420 1756 1966 1967 HSA/kex2 downstream of HSA/kex2leader and upstream of mature HSA. 314 2902pSAC35:Somatostatin(S14(A-G)).HSA A 14 amino acid peptide ofSomatostatin, pScCHSA 1589 1421 1757 1968 1969 HSA/kex2 an inhibitor ofgrowth hormone, synthesized as a C-terminal HSA fusion. Somatostatin hasan alanine to glycine change at amino acid 1 of SEQ ID NO: 1757. 3152903 pSAC35:HSA.A18-P202.IL22 Amino acids A18-P202 of IL22 fused pSAC351590 1422 1758 1970 1971 HSA downstream of full length HSA. 316 2904pSAC35:GLP-1(9-36).GLP-1(7-36).HSA Amino acids E100 to R127 of pScCHSA1234 1219 1249 1267 1268 HSA/kex2 preproglucagon (SEQ ID NO: 1249)(hereinafter, this particular mutant is referred to as GLP-1(9-36)) isfused downstream from the HSA/kex2 signal sequence and upstream fromGLP-1(7- 36), and mature HSA. 317 2908 pSAC35:HSA.HCE1P80 Mature HSAfused downstream of the pSAC35 1591 1423 1759 1972 1973 HSA/kex2HSA/kex2 leader and upstream of HCE1P80. 318 2909 pSAC35:HSA.HDRMI82Mature HSA fused downstream of the pSAC35 1592 1424 1760 1974 1975HSA/kex2 HSA/kex2 leader sequence and upstream of HDRMI82. 319 2910pSAC35:HSA.RegIV Mature HSA fused downstream of the pSAC35 1593 14251761 1976 1977 HSA/kex2 HSA/kex2 leader sequence and upstream of RegIV.320 2915 pC4:HSA#65.humancalcitonin.C1-G33 Modified HSA leader #65followed by pC4 1594 1426 1762 1978 1979 Modified mature HSA and C98through G130 of HSA #65 SEQ ID NO: 1762. 321 2930pC4.MPIF.Insulin(GYG).HSA Insulin is downstream of an MPIF signal pC41595 1427 1763 1980 1981 MPIF peptide and upstream of mature HSA. 3222931 pC4.HSA.Insulin(GYG) Synthetic gene coding for a mature pC4 15961428 1764 1982 1983 Modified single-chain insulin fused downstream ofHSA (A14) the modified HSA A14 leader and mature leader HSA. 323 2942pSac35.TA57.Insulin(GYG).HSA The TA57 Propeptide fused to a singlepScNHSA 1597 1429 1765 1984 1985 TA57 chain insulin (GYG), and thenmature propeptide HSA. 324 2943 pSAC35:HSA.T7.T7.T74-L98 Dimerconstruct- HSA/kex2 leader pScNHSA 1598 1430 1766 1986 1987 HSA/kex2followed by mature HSA followed by two copies of T7 peptide (SEQ ID NO:1766) of Tumstatin. 325 2944 pSAC:HSA.T8.T8.K69-S95 HSA/kex2 leaderfollowed by mature pScNHSA 1599 1431 1767 1988 1989 HSA/kex2 HSAfollowed by two copies of T8 peptide (SEQ ID NO: 1767) of Tumstatin 3262945 pSAC35:GLP-1(7-36(A8S)).GLP-1(7-36).HSA Amino acids H98 to R127 ofpScCHSA 1235 1220 1250 1269 1270 HSA/kex2 preproglucagon (SEQ ID NO:1250) is mutated at position 99 from alanine to serine (hereinafter,this particular mutant is referred to as GLP-1(7-36(A8S)), which isfused downstream from the HSA/kex2 signal sequence and upstream fromGLP-1(7-36), and mature HSA. 327 2946 pSAC:T1249(x2).HSA This dimerrepresents the wild type pScCHSA 1600 1432 1768 1990 1991 HSA/kex2sequence for T1249. Both dimers have been yeast codon optimized. Thesecond dimer was optimized to be different from the first (at the wobbleposition) to ensure good amplification. Construct has the HSA/kex2leader followed by T1249 dimer followed by mature HSA. 328 2947pSAG:CKb-1δ8(x2).HSA Invertase signal peptide followed by pSAC35 16011433 1769 1992 1993 invertase amino acids G28-N93 of full length CKβ1(SEQ IDNO: 1769), tandemly repeated, followed by mature HSA. 329 2964pSAC35:GLP-1(7-36)x2.HSA GLP-1(7-36) is tandemly repeated as a pSAC351236 1221 1251 1271 1272 HSA/kex2 dimer and fused downstream from theHSA/kex2 leader sequence and upstream from mature HSA. 330 2965pC4:MPIFspP.PTH(1-34).HSA MPIF signal peptide followed by 34 pC4 16021434 1770 1994 1995 MPIF amino acids of PTH followed by mature HSA. 3312966 pEE12:MPIFsp.PTH(l-34).HSA MPIF signal peptide followed by 34PEE12.1 1603 1435 1771 1996 1997 MPIF amino acids of PTH followed bymature HSA. 332 2982 pSAC35:GLP-1(7-36(A8G).GLP-1(7-36).HSAGLP-1(7-36(A8G)) (SEQ ID NO: 1808) is pScCHSA 1237 1222 1252 1273 1274HSA/kex2 fused downstream from the HSA/kex2 signal sequence and upstreamfrom GLP-1(7-36) and mature HSA. 333 2983 pC4.HSA.Growth Modified (A14)HSA leader followed by pC4 1604 1436 1772 1998 1999 ModifiedHormone.F27-F-217 mature HSA followed by F27 through HSA (A14) F217 ofgrowth hormone (corresponding to amino acids F1 to F191 of SEQ ID NO:1772). 334 2986 pSac35.y3SP.TA57PP.Insulin(GYG).HSA The TA57 Propeptidefused to a single pScCHSA 1605 1437 1773 2000 2001 TA57 chain insulin(GYG), and then mature propeptide HSA. 335 3025 pSAC35:INU.Insulin.HSAInulinase signal peptide is fused pScCHSA 1606 1438 1774 2002 2003inulinase upstream of single chain insulin (GYG) and HSA. 336 3027pSAC35:INV.GLP-1(7-36A8G)x2.HSA Invertase signal peptide followed bypSAC35 1607 1439 1775 2004 2005 invertase GLP-1(7-36(A8G)) (SEQ ID NO:1808) tandemly repeated as a dimer, followed by mature HSA. 337 3028pSAC35:INV.GLP-1(7-36(A8G)).GLP-1(7-36).HSA Invertase signal peptidefollowed by pSAC35 1608 1440 1776 2006 2007 invertase GLP-1(7-36(A8G))(SEQ ID NO: 1808), then GLP-1(7-36(A8G)), and then mature HSA. 338 3045pSAC35:DeltaKex.GLP-1(7-36A8G)x2.HSA HSA/kex2 signal sequence, minus thelast pSAC35 1609 1440 1776 2008 2009 HSA/kex2 six amino acids of theleader, is fused to last six GLP-1(7-36(A8G)) (SEQ ID NO: 1808) aminoacids which is tandemly repeated as a dimer, followed by mature HSA. 3393046 pSAC35:DeltaKex.GLP-1(7-36A8G).GLP-1(7-36).HSA HSA/kex2 signalsequence, minus the last pSAC35 1610 1440 1776 2010 2011 HSA/kex2 sixamino acids of the leader, is fused to last six GLP-1(7-36(A8G)) (SEQ IDNO: 1808), amino acids GLP-1(7-36), and mature HSA. 340 3047pSAC35:HSA.Tum5 Full length HSA fused to the Tum5 pScNHSA 1611 1443 17792012 2013 HSA peptide (SEQ ID NO: 1779) of Tumstatin. 341 3048pSAC35:Tum5.HSA. The Tum5 peptide (SEQ ID NO: 1780) of pScCHSA 1612 14441780 2014 2015 HSA/kex2 Tumstatin is fused to HSA and HSA/kex2 leader.342 3049 pC4.HSA.HCE1P80.D92-L229 Amino acids D92 to L229 of HCE1P80 pC41613 1445 1781 2016 2017 HSA are fused downstream of the full lengthHSA. 343 3050 pC4.HSA.HCE1P80.A20-L229 Amino acids A20-L229 of HCE1P80are pC4 1614 1446 1782 2018 2019 HSA fused downstream of the full lengthhuman HSA 344 3051 pSAC35.HSA.HCE1P80.D92-L229 Amino acids D92 to L229of HCE1P80, a pSAC35 1615 1447 1783 2020 2021 HSA member of the C1qfamily of proteins, are fused downstream of the full length human HSA345 3052 pSAC35.HSA.HCE1P80.A20-L229 Amino acids A20-L229 of HCE1P80 arepSAC35 1616 1448 1784 2022 2023 HSA fused downstream of the full lengthhuman HSA 346 3053 pC4.HSA.HDALV07.K101-N244 The globular domain ofadiponectin pC4 1617 1449 1785 2024 2025 HSA (amino acids K101-N244) hasbeen inserted downstream of full length human HSA 347 3055pSAC35.HSA.HDALV07(GD) Full length HSA followed by amino pSAC35 16181450 1786 2026 2027 HSA acids K101-N244 of HDALV07(GD)/ Adiponectin. 3483056 pSAC35.HSA.HDALV07.MP Full length HSA followed by amino acidspSAC35 1619 1451 1787 2028 2029 HSA Q18 to N244 of HDALV07. 349 3066pSAC35:CKB-1d8.GLP-1(7-36).HSA Invertase signal peptide followed bypScCHSA 1620 1452 1788 2030 2031 invertase amino acids G28-N93 of fulllength CKβ1 (SEQ IDNO: 1788), followed by GLP-1(7-36), followed bymature HSA. 350 3069 pSAC35:INU.GLP-1(7-36(A8G))x2.HSA The inulinasesignal sequence is fused to pSAC35 1621 1453 1789 2032 2033 inulinaseGLP-1(7-36(A8G)) (SEQ ID NO: 1808), which is tandemly repeated as adimer and fused to mature HSA. 351 3070 pSAC35:KT.GLP-1(7-36(A8G))x2.HSAGLP-1(7-36(A8G)) (SEQ ID NO: 1808) is pSAC35 1280 1281 1282 1283 1284Killer toxin tandemly repeated as a dimer and fused upstream from matureHSA and downstream from the killer toxin signal sequence. 352 3071pSAC35:MAF.GLP-1(7-36(A8G))x2.HSA The yeast mating factor α-1(hereinafter pSAC35 1622 1454 1790 2034 2035 MFα-1 MFα-1) signalsequence is fused to tandemly repeated copies of GLP-1(7- 36(A8G)) (SEQID NO: 1808), which are fused to mature HSA. 353 3072pSAC35:AP.GLP-1(7-36(A8G))x2.HSA The acid phosphatase signal sequence ispSAC35 1623 1455 1791 2036 2037 Acid fused to tandemly repeated copiesof phosphatase GLP-1(7-36(A8G)) (SEQ ID NO: 1808), which are fused tomature HSA. 354 3085 pSAC35:MAF.GLP-1(7-6(A8G)).GLP-1(7-36).HSA Theyeast mating factor α-1 (hereinafter pSAC35 1624 1456 1792 2038 2039MFα-1 MFα-1) signal sequence is fused to GLP-1(7-36(A8G)) (SEQ ID NO:1808), GLP-1(7-36), and mature HSA. 355 3086pSAC35:INU.GLP-1(7-36(A8G)).GLP-1(7-36).HSA The inulinase signalsequence is fused to pSAC35 1625 1457 1793 2040 2041 inulinaseGLP-1(7-36(A8G)) (SEQ ID NO: 1808), GLP-1(7-36), and mature HSA. 3563087 pSAC35:AP.GLP-1(7-36(A8G)).GLP-1(7-36).HSA The acid phosphatasesignal sequence is pSAC35 1626 1458 1794 2042 2043 Acid fused toGLP-1(7-36(A8G)) (SEQ ID phosphatase NO: 1808), GLP-1(7-36), and matureHSA. 357 3088 pSAC35.HSA.C-Peptide HSA/kex2 signal peptide, followed bypSAC35 1627 1459 1795 2044 2045 HSA/kex2 HSA, followed by the C-Peptidesequence. 358 3105 pSAC35:INV.t9HCC-l.G28-N93:spc.HSA Invertase signalpeptide followed by pSAC35 1628 1460 1796 2046 2047 invertase aminoacids G28 to N93 of HCC-1 fused upstream of a spacer and mature HSA. 3593106 pSACHSA.HCBOG68 mature HCBOG68 fused downstream of pSAC35 1629 14611797 HSA/kex2 mature HSA and the HSA/kex2 leader sequence. 360 3108pSAC35HSA.PYY Mature PYY fused downstream of mature pSAC35 1630 14621798 HSA/kex2 HSA and the HSA/kex2 leader. 361 3109 pSAC35HSA.PYY3-36HSA/kex2 leader followed by mature pSAC35 1631 1463 1799 HSA/kex2 HSAand then PYY3-36 (SEQ ID NO: 1799). 362 3117 pC4:PYY3-36/HSA HSA leaderfollowed by PYY3-36 (SEQ pC4 1632 1464 1800 2048 2049 HSA ID NO: 1800)and mature HSA. 363 3118 pSAC35:PYY3-36/HSA HSA/kex2 leader followed byPYY3-36 pSAC35 1633 1465 1801 2050 2051 HSA/kex2 (SEQ ID NO: 1801) andmature HSA. 364 3119 pSAC35:BNP/HSA HSA/kex2 leader followed by BNP andpSAC35 1634 1466 1802 2052 2053 HSA/kex2 mature HSA. 365 3124pSAC35:INV.CKB1.P29-N93:HSA Invertase signal peptide followed by pSAC351635 1467 1803 2054 2055 invertase amino acids 29 to 93 of full lengthckbeta1 fused to N-terminus of HSA. 366 3125pSAC35:INV.CKb-l.R27-N93:HSA Invertase signal peptide followed by pSAC351636 1468 1804 2056 2057 invertase amino acids 27 to 93 of full lengthckbeta1 fused to N-terminus of HSA. 367 3133pSac35.ySP.TA57PP.Insulin(GYG).HSA Variant TA57 propeptide leaderfollowed pSAC35 1637 1469 1805 2058 2059 TA57 by single chain insulin,followed by variant 1 mature HSA. 368 3134pSac35.ySP.TA57PP+S.Insulin(GYG).HSA Variant TA57 propeptide leaderfollowed pSAC35 1638 1470 1806 2060 2061 TA57 by single chain insulin,followed by variant 2 mature HSA. 369 3139pSAC35:INV.CKB1.G28-N93.DAHK.HSA Invertase signal peptide followed bypSAC35 1639 1471 1807 2062 2063 invertase amino acids G28-N93 of fulllength CKβ1 (see, e.g, SEQ IDNO: 1788), followed by a 16 amino acidlinker derived from the N-terminus of HSA, followed by mature HSA. 3703140 pSAC35:GLP1(mut)DAHK.HSA GLP-1(7-36(A8G)) (SEQ ID NO: 1808) ispSAC35 1640 1472 1808 2064 2065 HSA/kex2 linked to mature HSA by a 16amino acid linker derived from the N-terminus of HSA. The HSA/kex2signal sequence is used. 371 3141 pSAC35:Wnt10b/HSA HSA/kex2 leaderfollowed by amino pSAC35 1641 1473 1809 2066 2067 HSA/kex2 acids N29 toK389 of Wnt10b followed by mature HSA. 372 3142 pSAC35:Wnt11/HSAHSA/kex2 leader followed by mature pSAC35 1642 1474 1810 2068 2069HSA/kex2 Wnt11 followed by mature HSA. 373 3143 pSAC35:herstatin/HSAHSA/kex2 leader followed by amino pSAC35 1643 1475 1811 2070 2071HSA/kex2 acids T23 to G419 of herstatin followed by mature HSA. 374 3144pSAC35:adrenomedullin(27-52)/HSA HSA/kex2 leader followed by aminopSAC35 1644 1476 1812 2072 2073 HSA/kex2 acids 27-52 of adrenomedullinfollowed by mature HSA. 375 3149 pSAC35.HSA.C-peptide tandem Full lengthHSA fused to amino acids E7 pSAC35 1645 1477 1813 2074 2075 HSA to Q37of SEQ ID NO: 1813, tandemly repeated. 376 3152pSAC35:INV.CKB1.Met.R27-N93.HSA Invertase signal peptide followed by apSAC35 1646 1478 1814 2076 2077 invertase Met, followed by amino acidsR27-N93 of full length CKβl, followed by mature HSA. 377 3153pSAC35:INV.CKB1.Met.S26-N93.HSA Invertase signal peptide followed by apSAC35 1647 1479 1815 2078 2079 invertase Met, followed by amino acidsS26-N93 of full length CKβl, followed by mature HSA. 378 3154pSAC35:INV.CKB1.Met.S25-N93.HSA Invertase signal peptide followed by apSAC35 1648 1480 1816 2080 2081 invertase Met, followed by amino acidsS25-N93 of full length CKβl, followed by mature HSA. 379 3155pSAC35:INV.CKB1.Met.G28-N93.HSA Invertase signal peptide followed by aMet, pSAC35 1649 1481 1817 2082 2083 invertase followed by amino acidsG28-N93 of full length CKβl, followed by mature HSA. 380 3156pSAC35:INV.CKB1.Met.P29-N93.HSA Invertase signal peptide followed by aMet, pSAC35 1650 1482 1818 2084 2085 invertase followed by amino acidsP29-N93 of full length CKβl, followed by mature HSA. 381 3163pSAC35:HSA.hGH HSA/kex2 leader fused upstream of pSAC35 1303 1304 1305HSA/kex2 mature HSA and 191 amino acids of hGH. 382 3165 pSAC35:HSA.IFNaHSA fused upstream of IFNα and pSAC35 1300 1301 1302 HSA/kex2 also nameddownstream of the HSA/kex2 leader. CID 3165, pSAC35:HSA.INFα 383 3166pC4:MPIF1.A22-N93.HSA Amino acids A49 to N120 of MPIF (SEQ pC4 1651 14831819 2086 2087 MPIF ID NO: 1821) is fused downstream of MPIF signalpeptide and upstream of mature HSA. 384 3167 pC4:HSA.MPIF1.D45-N120 Fulllength HSA followed by amino acids pC4 1652 1484 1820 2088 2089 HSA D45through N120 of MPIF. 385 3168 PC4:MPIF-1.HSA Amino acids D45 throughN120 of MPIF pC4 1653 1485 1821 2090 2091 MPIF fused downstream of theMPIF signal sequence and upstream of mature HSA. 386 3169pSAC35:KT.CKB1.G28-N93.HSA Killer toxin signal sequence fused pSAC351654 1486 1822 Killer toxin upstream of amino acids G28 through N93 ofCKB1 (fragment shown as amino acids G1 to N66 of SEQ ID NO: 1822) andmature HSA. 387 3170 pSAC35:KT.HA.CKB1.G28-N93.HSA Killer toxin signalsequence followed by pSAC35 1655 1487 1823 Killer toxin HA dipeptide andamino acids G28 through N93 of CKB1 (fragment shown as amino acids G1 toN66 of SEQ ID NO: 1823) and mature HSA. 388 3171pSAC35:sCNTF(M1-G185):HSA C-terminal deletion of CNTF (amino pSAC35 16561488 1824 2092 2093 HSA/kex2 acids M1 through G185), fused upstream ofmature HSA and codon optimized for expression in yeast. HSA/kex2 signalsequence is used. 389 3172 pSAC35:HSA:sCNTF(M1-G185) HSA/kex2 signalsequence followed by pSAC35 1657 1489 1825 2094 2095 HSA/kex2 mature HSAand M1 through G185 of CNTF. 390 3184 pC4:HSA.NOGOR.C27-C309 Full lengthHSA followed by amino pC4 1658 1490 1826 2096 2097 HSA acids C27 to C309of the NOGO receptor. 391 3185 pC4.NOGOR.M1-C309.HSA Amino acids M1-C309of NOGO pC4 1659 1491 1827 2098 2099 Native receptor fused upstream ofmature HSA. NOGO receptor 392 3194 pC4:HSA(A14)-EPO(A28-D192.G140)codonopt Codon optimized EPO(A28-D192.G140) pC4 1660 1492 1828 2100 2101modified fused downstream of mature HSA with a HSA (A14) modified HSA(A14) signal sequence. 393 3195 pC4:HSA(S14)-EPO(A28-D192.G140)codon optCodon optimized EPO(A28-D192.G140) pC4 1661 1493 1829 2102 2103 modifiedfused downstream of mature HSA and a HSA (S14) modified HSA (S14) signalsequence. 394 3196 pC4:HSA(G14)-EPO(A28-D192.G140)codon opt Codonoptimized EPO(A28-D192.G140) pC4 1662 1494 1830 2104 2105 modified fuseddownstream of mature HSA with a (G14) modified (G14) HSA signalsequence. 395 3197 pC4.MPIF.Insulin(EAE).HSA A single-chain insulin isdownstream of pC4 1663 1495 1831 MPIF the MPIF signal peptide andupstream of mature human HSA. 396 3198 pSac35.INV.insulin(EAE).HSASingle-chain insulin is downstream of the pSAC35 1664 1496 1832invertase invertase signal peptide and upstream of mature human HSA 3973202 pSAC35:API.d8CKb1/HSA HSA/kex2 leader followed by amino pSAC35 16651497 1833 2106 2107 HSA/kex2 acids “API” followed by dSCKb1 and matureHSA. The sequence of delta 8 for CKB1 is shown in SEQ ID NO: 1833. 3983203 pSAC35:ASL.d8CKb1/HSA HSA/kex2 leader followed by amino pSAC35 16661498 1834 2108 2109 HSA/kex2 acids “ASL” followed by dSCKb1 and matureHSA. 399 3204 pSAC35:SPY.d8CKb1/HSA HSA/kex2 leader followed by aminopSAC35 1667 1499 1835 2110 2111 HSA/kex2 acids “SPY” followed by dSCKb1and mature HSA. 400 3205 pSAC35:MSPY.d8CKb1/HSA HSA/kex2 leader followedby amino pSAC35 1668 1500 1836 2112 2113 HSA/kex2 acids “MSPY” followedby dSCKb1 and mature HSA. 401 3206 pSAC35:CPYSC.d8CKb1/HSA HSA/kex2leader followed by a five pSAC35 1669 1501 1837 2114 2115 HSA/kex2 aminoacid linker followed by dSCKb1 and mature HSA. 402 3207pSAC35:GPY.d8CKb1/HSA HSA/kex2 leader followed by amino pSAC35 1670 15021838 2116 2117 HSA/kex2 acids “GPY” followed by dSCKb1 and mature HSA.403 3208 pSAC35:defensin alpha1/HSA Amino acids A65-C94 of defensinalpha pSAC35 1285 1286 1287 1288 1289 HSA/kex2 1 fused downstream of theHSA/kex2 leader and upstream of mature HSA. 404 3209 pSAC35:defensinalpha2/HSA Amino acids C66-C94 of defensin alpha 2 pSAC35 1290 1291 12921293 1294 HSA/kex2 fused downstream of the HSA/kex2 leader and upstreamof mature HSA. 405 3210 pSAC35:defensin alpha3/HSA Amino acids 65-94 ofSEQ ID NO1297, with pSAC35 1295 1296 1297 1298 1299 HSA/kex2 A65D andF92I mutations, fused downstream of the HSA/kex2 leader and upstream ofmature HSA. 406 3232 pSAC35:CART/HSA HSA/kex2 leader followed byprocessed pSAC35 1671 1503 1839 2118 2119 HSA/kex2 activecocaine-amphetamine regulated transcript (CART) (amino acids V69 throughL116) followed by mature HSA. 407 3238 pSAC35:phosphatonin.HSAPhosphatonin fused upstream of HSA. pSAC35 1306 1307 1308 Nativephosphatonin 408 3270 pSAC35:adipokine/HSA HSA/kex2 leader followed byadipokine pSAC35 1672 1504 1840 2120 2121 HSA/kex2 followed by matureHSA. 409 3272 pSAC35.INV:{D}8CK{b}1(x2)/HSA CKbeta-1 tandem repeat (x2)fusion to the pSAC35 1673 1505 1841 2122 2123 invertase N-termal HSA.Under the invertase signal peptide. 410 3274 pSAC35:P1pal-12.HSAP1pal-12 pepducin peptide fused upstream of pSAC35 1334 1335 1336HSA/kex2 mature HSA, and downstream of the HSA/kex2 leader sequence. 4113275 pSAC35:P4pal-10.HSA P4pal-10 pepducin peptide fused upstream ofpSAC35 1337 1338 1339 HSA/kex2 mature HSA, and downstream of theHSA/kex2 leader sequence. 412 3281 pSAC35.PY3-36(x2)/HSA PYY3-36 tandemrepeat (x2) fused pSAC35 1674 1506 1842 2124 2125 HSA/kex2 upstream ofHSA and downstream of the HSA/kex2 signal peptide. 413 3282pSAC35:HSA/PYY3-36(x2) PYY3-36 tandem repeat (x2) fused pSAC35 1675 15071843 2126 2127 HSA/kex2 downstream of mature HSA and HSA/kex2 leader.414 3298 pSAC35:IL21/HSA Amino acids Q30-S162 of IL-21 fused pSAC35 21672157 2177 2188 2189 HSA/Kex2 upstream of mature HSA and downstream ofHSA/kex2 leader 415 3307 pSAC35:IL4/HSA Amino acids H25-S153 of IL-4fused pSAC35 2168 2158 2178 2190 2191 HSA/Kex2 upstream of mature HSAand downstream of HSA/kex2 leader 416 3309pSAC:KT.GLP-1(7-36(A8G))x2.MSA.E25-A608 Killer toxin leader sequencefollowed by pSAC35 2170 2160 2180 2194 2195 Killer toxin GLP-1(7-36(A8G)followed by mature mouse serum albumin. 417 3312 pSAC35:hOCIL/HSAHSA/kex2 leader followed by amino acids N20 to pSAC35 2171 2161 21812196 2197 HSA/Kex2 V149 of hOCIL followed by mature HSA 418 7777 T20:HSAT20 fused downstream of full length HSA pC4 1170 1171 1172 HSA 419 8888pC4:BNP.HSA Human B-type natriuretic peptide fused pC4 1275 1276 12771278 1279 Native upstream of mature HSA. BNP 420 9999 T1249:HSA T1249fused downstream of full length HSA pC4 1173 1174 1175 HSA

Table 2 provides a non-exhaustive list of polynucleotides of theinvention comprising, or alternatively consisting of, nucleic acidmolecules encoding an albumin fusion protein. The first column, “FusionNo.” gives a fusion number to each polynucleotide. Column 2, “ConstructID” provides a unique numerical identifier for each polynucleotide ofthe invention. The Construct IDs may be used to identify polynucleotideswhich encode albumin fusion proteins comprising, or alternativelyconsisting of, a Therapeutic protein portion corresponding to a givenTherapeutic Protein:X listed in the corresponding row of Table 1 whereinthat Construct ID is listed in column 5. The “Construct Name” column(column 3) provides the name of a given albumin fusion construct orpolynucleotide.

The fourth column in Table 2, “Description” provides a generaldescription of a given albumin fusion construct, and the fifth column,“Expression Vector” lists the vector into which a polynucleotidecomprising, or alternatively consisting of, a nucleic acid moleculeencoding a given albumin fusion protein was cloned. Vectors are known inthe art, and are available commercially or described elsewhere. Forexample, as described in the Examples, an “expression cassette”comprising, or alternatively consisting of, one or more of (1) apolynucleotide encoding a given albumin fusion protein, (2) a leadersequence, (3) a promoter region, and (4) a transcriptional terminator,may be assembled in a convenient cloning vector and subsequently bemoved into an alternative vector, such as, for example, an expressionvector including, for example, a yeast expression vector or a mammalianexpression vector. In one embodiment, for expression in S. cervisiae, anexpression cassette comprising, or alternatively consisting of, anucleic acid molecule encoding an albumin fusion protein is cloned intopSAC35. In another embodiment, for expression in CHO cells, anexpression cassette comprising, or alternatively consisting of, anucleic acid molecule encoding an albumin fusion protein is cloned intopC4. In a further embodiment, a polynucleotide comprising oralternatively consisting of a nucleic acid molecule encoding theTherapeutic protein portion of an albumin fusion protein is cloned intopC4:HSA. In a still further embodiment, for expression in NS0 cells, anexpression cassette comprising, or alternatively consisting of, anucleic acid molecule encoding an albumin fusion protein is cloned intopEE12. Other useful cloning and/or expression vectors will be known tothe skilled artisan and are within the scope of the invention.

Column 6, “SEQ ID NO:Y,” provides the full length amino acid sequence ofthe albumin fusion protein of the invention. In most instances, SEQ IDNO:Y shows the unprocessed form of the albumin fusion protein encoded—inother words, SEQ ID NO:Y shows the signal sequence, a HSA portion, and atherapeutic portion all encoded by the particular construct.Specifically contemplated by the present invention are allpolynucleotides that encode SEQ ID NO:Y. When these polynucleotides areused to express the encoded protein from a cell, the cell's naturalsecretion and processing steps produces a protein that lacks the signalsequence listed in columns 4 and/or 11 of Table 2. The specific aminoacid sequence of the listed signal sequence is shown later in thespecification or is well known in the art. Thus, most preferredembodiments of the present invention include the albumin fusion proteinproduced by a cell (which would lack the leader sequence shown incolumns 4 and/or 11 of Table 2). Also most preferred are polypeptidescomprising SEQ ID NO:Y without the specific leader sequence listed incolumns 4 and/or 11 of Table 2. Compositions comprising these twopreferred embodiments, including pharmaceutical compositions, are alsopreferred. Moreover, it is well within the ability of the skilledartisan to replace the signal sequence listed in columns 4 and/or 11 ofTable 2 with a different signal sequence, such as those described laterin the specification to facilitate secretion of the processed albuminfusion protein.

The seventh column, “SEQ ID NO:X,” provides the parent nucleic acidsequence from which a polynucleotide encoding a Therapeutic proteinportion of a given albumin fusion protein may be derived. In oneembodiment, the parent nucleic acid sequence from which a polynucleotideencoding a Therapeutic protein portion of an albumin fusion protein maybe derived comprises the wild type gene sequence encoding a Therapeuticprotein shown in Table 1. In an alternative embodiment, the parentnucleic acid sequence from which a polynucleotide encoding a Therapeuticprotein portion of an albumin fusion protein may be derived comprises avariant or derivative of a wild type gene sequence encoding aTherapeutic protein shown in Table 1, such as, for example, a syntheticcodon optimized variant of a wild type gene sequence encoding aTherapeutic protein.

The eighth column, “SEQ ID NO:Z,” provides a predicted translation ofthe parent nucleic acid sequence (SEQ ID NO:X). This parent sequence canbe a full length parent protein used to derive the particular construct,the mature portion of a parent protein, a variant or fragment of awildtype protein, or an artificial sequence that can be used to createthe described construct. One of skill in the art can use this amino acidsequence shown in SEQ ID NO:Z to determine which amino acid residues ofan albumin fusion protein encoded by a given construct are provided bythe therapeutic protein. Moreover, it is well within the ability of theskilled artisan to use the sequence shown as SEQ ID NO:Z to derive theconstruct described in the same row. For example, if SEQ ID NO:Zcorresponds to a full length protein, but only a portion of that proteinis used to generate the specific CID, it is within the skill of the artto rely on molecular biology techniques, such as PCR, to amplify thespecific fragment and clone it into the appropriate vector.

Amplification primers provided in columns 9 and 10, “SEQ ID NO:A” and“SEQ ID NO:B” respectively, are exemplary primers used to generate apolynucleotide comprising or alternatively consisting of a nucleic acidmolecule encoding the Therapeutic protein portion of a given albuminfusion protein. In one embodiment of the invention, oligonucleotideprimers having the sequences shown in columns 9 and/or 10 (SEQ ID NOS:Aand/or B) are used to PCR amplify a polynucleotide encoding theTherapeutic protein portion of an albumin fusion protein using a nucleicacid molecule comprising or alternatively consisting of the nucleotidesequence provided in column 7 (SEQ ID NO:X) of the corresponding row asthe template DNA. PCR methods are well-established in the art.Additional useful primer sequences could readily be envisioned andutilized by those of ordinary skill in the art.

In an alternative embodiment, oligonucleotide primers may be used inoverlapping PCR reactions to generate mutations within a template DNAsequence. PCR methods are known in the art.

As shown in Table 3, certain albumin fusion constructs disclosed in thisapplication have been deposited with the ATCC®.

TABLE 3 Construct ID Construct Name ATCC Deposit No./Date 1642pSAC35:GCSF.T31-P204.HSA PTA-3767 Oct. 5, 2001 1643pSAC35:HSA.GCSF.T31-P204 PTA-3766 Oct. 5, 2001 1812pSAC35:IL2.A21-T153.HSA PTA-3759 Oct. 4, 2001 1941 pC4:HSA/PTH84(junctioned) PTA-3761 Oct. 4, 2001 1949 pC4:PTH.S1-Q84/HSA (junctioned)PTA-3762 Oct. 4, 2001 1966 pC4:EPO.M1-D192.HSA PTA-3771 also namedpC4:EPOM1-D192.HSA Oct. 5, 2001 1981 pC4.HSA-EPO.A28-D192 PTA-3770 Oct.5, 2001 1997 pEE12.1:EPOM1-D192.HSA PTA-3768 Oct. 5, 2001 2030pSAC35.ycoIL-2.A21-T153.HSA PTA-3757 Oct. 4, 2001 2031pSAC35.HSA.ycoIL-2.A21-T153 PTA-3758 Oct. 4, 2001 2053 pEE12:IFNb-HSAPTA-3764 also named pEE12.1:IFNβ-HSA Oct. 4, 2001 2054 pEE12:HSA-IFNbPTA-3941 Dec. 19, 2001 2249 pSAC35:IFNa2-HSA PTA-3763 also namedpSAC23:IFNα2-HSA Oct. 4, 2001 2250 pSAC35:HSA.INSULIN(GYG) PTA-3916 alsonamed pSAC35.HSA.INSULING(GYG).F1-N62 Dec. 7, 2001 2255pSAC35:INSULIN(GYG).HSA PTA-3917 also namedpSAC35.INSULING(GYG).F1-N62.HSA Dec. 7, 2001 2276pSAC35:HSA.INSULIN(GGG) PTA-3918 also named pSAC35.HSA.INSULING(GGG).F1-N58 Dec. 7, 2001 2298 pEE12.1:EPO.R140G.HSA PTA-3760 Oct. 4, 20012294 pC4:EPO.R140G.HSA PTA-3742 also named pC4.EPO.R1406.HSA Sep. 28,2001 2325 pC4.EPO:M1-D192.HSA.Codon opt. PTA-3773 Oct. 5, 2001 2343pSAC35.INV-IFNA2.HSA PTA-3940 Dec. 19, 2001 2363pC4.GCSF.HSA.EPO.A28-D192 PTA-3740 Sep. 28, 2001 2373pC4.GCSF.HSA.EPO.A28-D192.R140G PTA-3741 Sep. 28, 2001 2381pC4:HSA-IFNa2(C17-E181) PTA-3942 Dec. 19, 2001 2382 pC4:IFNa2-HSAPTA-3939 Dec. 19, 2001 2387 pC4:EPO(G140)-HSA-GCSF.T31-P204 PTA-3919Dec. 11, 2001 2414 pC4.EPO:M1-D192copt.HSA.GCSF.T31-P204 PTA-3924 alsonamed Dec. 12, 2001 pC4.EPO:M1-D192copt.HAS.GCSF.T31-P204 2441pEE12.EPO:M1-D192copt.HSA.GCSF.T31-P204 PTA-3923 also named: Dec. 12,2001 pEE12.EPO:M1-D192copt.HAS.GCSF.T31-P204 2492 pC4.IFNb(deltaM22).HSAPTA-3943 Dec. 19, 2001 3070 pSAC35:KT.GLP-1(7-36(A8G))x2.HSA PTA-4671Sep. 16, 2002 3165 pSAC35:HSA.IFNa PTA-4670 also named CID 3165,pSAC35:HSA.INFα Sep. 16, 2002 3163 pSAC35:HSA.hGH PTA-4770 Oct. 22, 2002

It is possible to retrieve a given albumin fusion construct from thedeposit by techniques known in the art and described elsewhere herein(see, Example 40). The ATCC is located at 10801 University Boulevard,Manassas, Va. 20110-2209, USA. The ATCC deposits were made pursuant tothe terms of the Budapest Treaty on the international recognition of thedeposit of microorganisms for the purposes of patent procedure.

In a further embodiment of the invention, an “expression cassette”comprising, or alternatively consisting of one or more of (1) apolynucleotide encoding a given albumin fusion protein, (2) a leadersequence, (3) a promoter region, and (4) a transcriptional terminatorcan be moved or “subcloned” from one vector into another. Fragments tobe subcloned may be generated by methods well known in the art, such as,for example, PCR amplification (e.g., using oligonucleotide primershaving the sequence shown in SEQ ID NO:A or B), and/or restrictionenzyme digestion.

In preferred embodiments, the albumin fusion proteins of the inventionare capable of a therapeutic activity and/or biologic activitycorresponding to the therapeutic activity and/or biologic activity ofthe Therapeutic protein corresponding to the Therapeutic protein portionof the albumin fusion protein listed in the corresponding row ofTable 1. In further preferred embodiments, the therapeutically activeprotein portions of the albumin fusion proteins of the invention arefragments or variants of the protein encoded by the sequence shown inSEQ ID NO:X column of Table 2, and are capable of the therapeuticactivity and/or biologic activity of the corresponding Therapeuticprotein.

Non-Human Albumin Fusion Proteins of Growth Hormone.

In one embodiment, the albumin fusion proteins of the invention compriseone or more Serum Albumin proteins of a non-human animal species, fusedin tandem and in-frame either at the N-terminus or the C-terminus to oneor more Growth Hormone proteins of the same non-human animal species.Non-human Serum Albumin and Growth Hormone proteins are well known inthe art and available in public databases. For example, Table 4 presentsaccession numbers corresponding to non-human Serum Albumin sequences(column 2) and non-human Growth Hormone sequences (column 3) found inGenBank. In a preferred embodiment, a Serum Albumin protein from anon-human animal species listed in Table 4 is fused to a Growth Hormoneprotein from the same non-human animal species.

In a specific embodiment, the albumin fusion protein of the inventioncomprises one or more Bos taurus Serum Albumin proteins listed in Table4, column 2, fused in tandem and in-frame either at the N-terminus orthe C-terminus to one or more Bos taurus Growth Hormone proteins listedin Table 4, column 3.

Fusion proteins comprising fragments or variants of non-human SerumAlbumin, such as, for example, the mature form of Serum Albumin, arealso encompassed by the invention. Fusion proteins comprising fragmentsor variants of non-human Growth Hormone proteins, such as, for example,the mature form of Growth Hormone, are also encompassed by theinvention. Preferably the non-human Growth Hormone fragments andvariants retain growth hormone activity.

Polynucleotides of the invention comprise, or alternatively consist of,one or more nucleic acid molecules encoding a non-human albumin fusionprotein described above. For example, the polynucleotides can comprise,or alternatively consist of, one or more nucleic acid molecules thatencode a Serum Albumin protein from a non-human animal species listed inTable 4, column 1 (such as, for example, the non-human Serum Albuminreference sequences listed in Table 4, column 2) fused in tandem andin-frame either 5′ or 3′ to a polynucleotide that comprises, oralternatively consists of, one or more nucleic acid molecules encodingthe non-human Growth Hormone protein of the corresponding non-humananimal species (for example, the Growth Hormone reference sequenceslisted in Table 4, column 3).

The above-described non-human albumin fusion proteins are encompassed bythe invention, as are host cells and vectors containing thesepolynucleotides. In one embodiment, a non-human albumin fusion proteinencoded by a polynucleotide as described above has extended shelf life.In an additional embodiment, a non-human albumin fusion protein encodedby a polynucleotide described above has a longer serum half-life and/ormore stabilized activity in solution (or in a pharmaceuticalcomposition) in vitro and/or in vivo than the corresponding unfusedGrowth Hormone molecule.

The present invention also encompasses methods of preventing, treating,or ameliorating a disease or disorder in a non-human animal species. Incertain embodiments, the present invention encompasses a method oftreating a veterinary disease or disorder comprising administering to anon-human animal species in which such treatment, prevention oramelioration is desired an albumin fusion protein of the invention thatcomprises a Growth Hormone portion corresponding to a Growth Hormoneprotein (or fragment or variant thereof) in an amount effective totreat, prevent or ameliorate the disease or disorder. Veterinarydiseases and/or disorders which may be treated, prevented, orameliorated include growth disorders (such as, for example, pituitarydwarfism), shin soreness, obesity, growth hormone-responsive dermatosis,dilated cardiomyopathy, eating disorders, reproductive disorders, andendocrine disorders.

Non-human albumin fusion proteins of the invention may also be used topromote healing of skin wounds, corneal injuries, bone fractures, andinjuries of joints, tendons, or ligaments.

Non-human albumin fusion proteins of the invention may also be used toincrease milk production in lactating animals. In a preferredembodiment, the lactating animal is a dairy cow.

Non-human albumin fusion proteins of the invention may also be used toimprove body condition in aged animals.

Non-human albumin fusion proteins of the invention may also be used toincrease fertility, pregnancy rates, and reproductive success indomesticated animals.

Non-human albumin fusion proteins of the invention may also be used toimprove the lean-to-fat ratio in animals raised for consumption, as wellas to improve appetite, and increase body size and growth rate.

TABLE 4 Non-Human Serum Albumin Reference Non-Human Sequence(s): GenBankProtein Non-Human Growth Hormone Reference Species Accession Nos.Sequence(s): GenBank Protein Accession Nos. Bos taurus ABBOS, CAA76847,P02769, STBO, BAA06379, A29864, AAF28806, CAA41735, 229552, AAA51411AAF28805, AAF28804, P01246, AAF03132, AAC63901, AAB92549, A36506,I45901, JC1316, CAA23445, CAA00787, CAA00598, AAA30547, AAA30546,AAA30545, AAA30544, AAA30543, AAA30542 Sus scrofa P08835, CAA30970,AAA30988 STPG, PC1017, AAB29947, AAB84359, I46585, I46584, PC1063,A01516, AAB17619, 226829, 225740, CAA37411, CAA00592, AAA73478,AAA73477, CAA00356, AAA31046, AAA31045, AAA31044, AA30543 Equus caballusABHOS, AAG40944, P35747, STHO, P01245, AAD25992, 227704, AAA21027CAA52194 Ovis aries ABSHS, P14639, CAA34903 STSH, AAB24467, AAC48679,228487, 223932, CAA34098, CAA31063, CAA00828, AAA31527 Salmo salarABONS2, ABONS2, CAA36643, STONC, P07064, Q07221, P48096, P10814,CAA43187 P10607, I51186, S03709, JS0179, A23154, S06489, CAA42431,AAB29165, AAB24612, Q91221, Q91222, CAA43942, CAA32481, 738042, 224555,CAA00427, AAA50757, AAA49558, AAA49555, AAA49553, AAA49401, AAA49406,AAA49403, AAA49402 Gallus gallus ABCHS, P19121, CAA43098 BAB62262,BAB69037, AAK95643, A60509, AAG01029, BAA01365, P08998, 226895,CAA31127, CAA35619, AAA48780 Felis catus P49064, S57632, CAA59279,JC4660 JC4632, P46404. AAC00073, AAA96142, AAA67294 Canis familiarisP49822, S29749, CAB64867, P33711, I46145, AAF89582, AAF21502, CAA76841,AAB30434 AAD43366, S35790, AAB34229, CAA80601

Polypeptide and Polynucleotide Fragments and Variants

Fragments

The present invention is further directed to fragments of theTherapeutic proteins described in Table 1, albumin proteins, and/oralbumin fusion proteins of the invention.

The present invention is also directed to polynucleotides encodingfragments of the Therapeutic proteins described in Table 1, albuminproteins, and/or albumin fusion proteins of the invention.

Even if deletion of one or more amino acids from the N-terminus of aprotein results in modification or loss of one or more biologicalfunctions of the Therapeutic protein, albumin protein, and/or albuminfusion protein of the invention, other Therapeutic activities and/orfunctional activities (e.g., biological activities, ability tomultimerize, ability to bind a ligand) may still be retained. Forexample, the ability of polypeptides with N-terminal deletions to induceand/or bind to antibodies which recognize the complete or mature formsof the polypeptides generally will be retained when less than themajority of the residues of the complete polypeptide are removed fromthe N-terminus. Whether a particular polypeptide lacking N-terminalresidues of a complete polypeptide retains such immunologic activitiescan readily be determined by routine methods described herein andotherwise known in the art. It is not unlikely that a mutein with alarge number of deleted N-terminal amino acid residues may retain somebiological or immunogenic activities. In fact, peptides composed of asfew as six amino acid residues may often evoke an immune response.

Accordingly, fragments of a Therapeutic protein corresponding to aTherapeutic protein portion of an albumin fusion protein of theinvention, include the full length protein as well as polypeptideshaving one or more residues deleted from the amino terminus of the aminoacid sequence of the reference polypeptide (i.e., a Therapeutic proteinreferred to in Table 1, or a Therapeutic protein portion of an albuminfusion protein encoded by a polynucleotide or albumin fusion constructdescribed in Table 2). In particular, N-terminal deletions may bedescribed by the general formula m to q, where q is a whole integerrepresenting the total number of amino acid residues in a referencepolypeptide (e.g., a Therapeutic protein referred to in Table 1, or aTherapeutic protein portion of an albumin fusion protein of theinvention, or a Therapeutic protein portion of an albumin fusion proteinencoded by a polynucleotide or albumin fusion construct described inTable 2), and m is defined as any integer ranging from 2 to q minus 6.Polynucleotides encoding these polypeptides are also encompassed by theinvention.

In addition, fragments of serum albumin polypeptides corresponding to analbumin protein portion of an albumin fusion protein of the invention,include the full length protein as well as polypeptides having one ormore residues deleted from the amino terminus of the amino acid sequenceof the reference polypeptide (i.e., serum albumin, or a serum albuminportion of an albumin fusion protein encoded by a polynucleotide oralbumin fusion construct described in Table 2). In preferredembodiments, N-terminal deletions may be described by the generalformula m to 585, where 585 is a whole integer representing the totalnumber of amino acid residues in mature human serum albumin (SEQ IDNO:1038), and m is defined as any integer ranging from 2 to 579.Polynucleotides encoding these polypeptides are also encompassed by theinvention. In additional embodiments, N-terminal deletions may bedescribed by the general formula m to 609, where 609 is a whole integerrepresenting the total number of amino acid residues in full lengthhuman serum albumin (SEQ ID NO:1094), and m is defined as any integerranging from 2 to 603. Polynucleotides encoding these polypeptides arealso encompassed by the invention.

Moreover, fragments of albumin fusion proteins of the invention, includethe full length albumin fusion protein as well as polypeptides havingone or more residues deleted from the amino terminus of the albuminfusion protein (e.g., an albumin fusion protein encoded by apolynucleotide or albumin fusion construct described in Table 2; or analbumin fusion protein having the amino acid sequence disclosed incolumn 6 of Table 2). In particular, N-terminal deletions may bedescribed by the general formula m to q, where q is a whole integerrepresenting the total number of amino acid residues in the albuminfusion protein, and m is defined as any integer ranging from 2 to qminus 6. Polynucleotides encoding these polypeptides are alsoencompassed by the invention.

Also as mentioned above, even if deletion of one or more amino acidsfrom the N-terminus or C-terminus of a reference polypeptide (e.g., aTherapeutic protein; serum albumin protein; or albumin fusion protein ofthe invention) results in modification or loss of one or more biologicalfunctions of the protein, other functional activities (e.g., biologicalactivities, ability to multimerize, ability to bind a ligand) and/orTherapeutic activities may still be retained. For example the ability ofpolypeptides with C-terminal deletions to induce and/or bind toantibodies which recognize the complete or mature forms of thepolypeptide generally will be retained when less than the majority ofthe residues of the complete or mature polypeptide are removed from theC-terminus. Whether a particular polypeptide lacking the N-terminaland/or C-terminal residues of a reference polypeptide retainsTherapeutic activity can readily be determined by routine methodsdescribed herein and/or otherwise known in the art.

The present invention further provides polypeptides having one or moreresidues deleted from the carboxy terminus of the amino acid sequence ofa Therapeutic protein corresponding to a Therapeutic protein portion ofan albumin fusion protein of the invention (e.g., a Therapeutic proteinreferred to in Table 1, or a Therapeutic protein portion of an albuminfusion protein encoded by a polynucleotide or albumin fusion constructdescribed in Table 2). In particular, C-terminal deletions may bedescribed by the general formula 1 to n, where n is any whole integerranging from 6 to q minus 1, and where q is a whole integer representingthe total number of amino acid residues in a reference polypeptide(e.g., a Therapeutic protein referred to in Table 1, or a Therapeuticprotein portion of an albumin fusion protein encoded by a polynucleotideor albumin fusion construct described in Table 2). Polynucleotidesencoding these polypeptides are also encompassed by the invention.

In addition, the present invention provides polypeptides having one ormore residues deleted from the carboxy terminus of the amino acidsequence of an albumin protein corresponding to an albumin proteinportion of an albumin fusion protein of the invention (e.g., serumalbumin or an albumin protein portion of an albumin fusion proteinencoded by a polynucleotide or albumin fusion construct described inTable 2). In particular, C-terminal deletions may be described by thegeneral formula 1 to n, where n is any whole integer ranging from 6 to584, where 584 is the whole integer representing the total number ofamino acid residues in mature human serum albumin (SEQ ID NO:1038)minus 1. Polynucleotides encoding these polypeptides are alsoencompassed by the invention. In particular, C-terminal deletions may bedescribed by the general formula 1 to n, where n is any whole integerranging from 6 to 608, where 608 is the whole integer representing thetotal number of amino acid residues in serum albumin (SEQ ID NO:1094)minus 1. Polynucleotides encoding these polypeptides are alsoencompassed by the invention.

Moreover, the present invention provides polypeptides having one or moreresidues deleted from the carboxy terminus of an albumin fusion proteinof the invention. In particular, C-terminal deletions may be describedby the general formula 1 to n, where n is any whole integer ranging from6 to q minus 1, and where q is a whole integer representing the totalnumber of amino acid residues in an albumin fusion protein of theinvention. Polynucleotides encoding these polypeptides are alsoencompassed by the invention.

In addition, any of the above described N- or C-terminal deletions canbe combined to produce a N- and C-terminal deleted referencepolypeptide. The invention also provides polypeptides having one or moreamino acids deleted from both the amino and the carboxyl termini, whichmay be described generally as having residues m to n of a referencepolypeptide (e.g., a Therapeutic protein referred to in Table 1, or aTherapeutic protein portion of an albumin fusion protein of theinvention, or a Therapeutic protein portion encoded by a polynucleotideor albumin fusion construct described in Table 2, or serum albumin(e.g., SEQ ID NO:1038), or an albumin protein portion of an albuminfusion protein of the invention, or an albumin protein portion encodedby a polynucleotide or albumin fusion construct described in Table 2, oran albumin fusion protein, or an albumin fusion protein encoded by apolynucleotide or albumin fusion construct of the invention) where n andm are integers as described above. Polynucleotides encoding thesepolypeptides are also encompassed by the invention.

The present application is also directed to proteins containingpolypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identicalto a reference polypeptide sequence (e.g., a Therapeutic proteinreferred to in Table 1, or a Therapeutic protein portion of an albuminfusion protein of the invention, or a Therapeutic protein portionencoded by a polynucleotide or albumin fusion construct described inTable 2, or serum albumin (e.g., SEQ ID NO: 1038), or an albumin proteinportion of an albumin fusion protein of the invention, or an albuminprotein portion encoded by a polynucleotide or albumin fusion constructdescribed in Table 2, or an albumin fusion protein, or an albumin fusionprotein encoded by a polynucleotide or albumin fusion construct of theinvention) set forth herein, or fragments thereof. In preferredembodiments, the application is directed to proteins comprisingpolypeptides at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identicalto reference polypeptides having the amino acid sequence of N- andC-terminal deletions as described above. Polynucleotides encoding thesepolypeptides are also encompassed by the invention.

Preferred polypeptide fragments of the invention are fragmentscomprising, or alternatively, consisting of, an amino acid sequence thatdisplays a Therapeutic activity and/or functional activity (e.g.biological activity) of the polypeptide sequence of the Therapeuticprotein or serum albumin protein of which the amino acid sequence is afragment.

Other preferred polypeptide fragments are biologically active fragments.Biologically active fragments are those exhibiting activity similar, butnot necessarily identical, to an activity of the polypeptide of thepresent invention. The biological activity of the fragments may includean improved desired activity, or a decreased undesirable activity.

Variants

“Variant” refers to a polynucleotide or nucleic acid differing from areference nucleic acid or polypeptide, but retaining essentialproperties thereof. Generally, variants are overall closely similar,and, in many regions, identical to the reference nucleic acid orpolypeptide.

As used herein, “variant”, refers to a Therapeutic protein portion of analbumin fusion protein of the invention, albumin portion of an albuminfusion protein of the invention, or albumin fusion protein of theinvention differing in sequence from a Therapeutic protein (e.g. see“therapeutic” column of Table 1), albumin protein, and/or albumin fusionprotein, respectively, but retaining at least one functional and/ortherapeutic property thereof as described elsewhere herein or otherwiseknown in the art. Generally, variants are overall very similar, and, inmany regions, identical to the amino acid sequence of the Therapeuticprotein corresponding to a Therapeutic protein portion of an albuminfusion protein, albumin protein corresponding to an albumin proteinportion of an albumin fusion protein, and/or albumin fusion protein.Nucleic acids encoding these variants are also encompassed by theinvention.

The present invention is also directed to proteins which comprise, oralternatively consist of, an amino acid sequence which is at least 80%,85%, 90%, 95%, 96%, 97%, 98%, 99% or 100%, identical to, for example,the amino acid sequence of a Therapeutic protein corresponding to aTherapeutic protein portion of an albumin fusion protein of theinvention (e.g., the amino acid sequence of a Therapeutic protein:Xdisclosed in Table 1; or the amino acid sequence of a Therapeuticprotein portion of an albumin fusion protein encoded by a polynucleotideor albumin fusion construct described in Table 1 and 2, or fragments orvariants thereof), albumin proteins corresponding to an albumin proteinportion of an albumin fusion protein of the invention (e.g., the aminoacid sequence of an albumin protein portion of an albumin fusion proteinencoded by a polynucleotide or albumin fusion construct described inTable 1 and 2; the amino acid sequence shown in SEQ ID NO: 1038; orfragments or variants thereof), and/or albumin fusion proteins.Fragments of these polypeptides are also provided (e.g., those fragmentsdescribed herein). Further polypeptides encompassed by the invention arepolypeptides encoded by polynucleotides which hybridize to thecomplement of a nucleic acid molecule encoding an albumin fusion proteinof the invention under stringent hybridization conditions (e.g.,hybridization to filter bound DNA in 6× Sodium chloride/Sodium citrate(SSC) at about 45 degrees Celsius, followed by one or more washes in0.2×SSC, 0.1% SDS at about 50-65 degrees Celsius), under highlystringent conditions (e.g., hybridization to filter bound DNA in 6×sodium chloride/Sodium citrate (SSC) at about 45 degrees Celsius,followed by one or more washes in 0.1×SSC, 0.2% SDS at about 68 degreesCelsius), or under other stringent hybridization conditions which areknown to those of skill in the art (see, for example, Ausubel, F. M. etal., eds., 1989 Current protocol in Molecular Biology, Green publishingassociates, Inc., and John Wiley & Sons Inc., New York, at pages6.3.1-6.3.6 and 2.10.3). Polynucleotides encoding these polypeptides arealso encompassed by the invention.

By a polypeptide having an amino acid sequence at least, for example,95% “identical” to a query amino acid sequence, it is intended that theamino acid sequence of the subject polypeptide is identical to the querysequence except that the subject polypeptide sequence may include up tofive amino acid alterations per each 100 amino acids of the query aminoacid sequence. In other words, to obtain a polypeptide having an aminoacid sequence at least 95% identical to a query amino acid sequence, upto 5% of the amino acid residues in the subject sequence may beinserted, deleted, or substituted with another amino acid. Thesealterations of the reference sequence may occur at the amino- orcarboxy-terminal positions of the reference amino acid sequence oranywhere between those terminal positions, interspersed eitherindividually among residues in the reference sequence or in one or morecontiguous groups within the reference sequence.

As a practical matter, whether any particular polypeptide is at least80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to, for instance, theamino acid sequence of an albumin fusion protein of the invention or afragment thereof (such as a Therapeutic protein portion of the albuminfusion protein or an albumin portion of the albumin fusion protein), canbe determined conventionally using known computer programs. A preferredmethod for determining the best overall match between a query sequence(a sequence of the present invention) and a subject sequence, alsoreferred to as a global sequence alignment, can be determined using theFASTDB computer program based on the algorithm of Brutlag et al. (Comp.App. Biosci. 6:237-245 (1990)). In a sequence alignment the query andsubject sequences are either both nucleotide sequences or both aminoacid sequences. The result of said global sequence alignment isexpressed as percent identity. Preferred parameters used in a FASTDBamino acid alignment are: Matrix=PAM 0, k-tuple=2, Mismatch Penalty=1,Joining Penalty=20, Randomization Group Length=0, Cutoff Score=1, WindowSize=sequence length, Gap Penalty=5, Gap Size Penalty=0.05, WindowSize=500 or the length of the subject amino acid sequence, whichever isshorter.

If the subject sequence is shorter than the query sequence due to N- orC-terminal deletions, not because of internal deletions, a manualcorrection must be made to the results. This is because the FASTDBprogram does not account for N- and C-terminal truncations of thesubject sequence when calculating global percent identity. For subjectsequences truncated at the N- and C-termini, relative to the querysequence, the percent identity is corrected by calculating the number ofresidues of the query sequence that are N- and C-terminal of the subjectsequence, which are not matched/aligned with a corresponding subjectresidue, as a percent of the total bases of the query sequence. Whethera residue is matched/aligned is determined by results of the FASTDBsequence alignment. This percentage is then subtracted from the percentidentity, calculated by the above FASTDB program using the specifiedparameters, to arrive at a final percent identity score. This finalpercent identity score is what is used for the purposes of the presentinvention. Only residues to the N- and C-termini of the subjectsequence, which are not matched/aligned with the query sequence, areconsidered for the purposes of manually adjusting the percent identityscore. That is, only query residue positions outside the farthest N- andC-terminal residues of the subject sequence.

For example, a 90 amino acid residue subject sequence is aligned with a100 residue query sequence to determine percent identity. The deletionoccurs at the N-terminus of the subject sequence and therefore, theFASTDB alignment does not show a matching/alignment of the first 10residues at the N-terminus. The 10 unpaired residues represent 10% ofthe sequence (number of residues at the N- and C-termini notmatched/total number of residues in the query sequence) so 10% issubtracted from the percent identity score calculated by the FASTDBprogram. If the remaining 90 residues were perfectly matched the finalpercent identity would be 90%. In another example, a 90 residue subjectsequence is compared with a 100 residue query sequence. This time thedeletions are internal deletions so there are no residues at the N- orC-termini of the subject sequence which are not matched/aligned with thequery. In this case the percent identity calculated by FASTDB is notmanually corrected. Once again, only residue positions outside the N-and C-terminal ends of the subject sequence, as displayed in the FASTDBalignment, which are not matched/aligned with the query sequence aremanually corrected for. No other manual corrections are to made for thepurposes of the present invention.

The variant will usually have at least 75% (preferably at least about80%, 90%, 95% or 99%) sequence identity with a length of normal HA orTherapeutic protein which is the same length as the variant. Homology oridentity at the nucleotide or amino acid sequence level is determined byBLAST (Basic Local Alignment Search Tool) analysis using the algorithmemployed by the programs blastp, blastn, blastx, tblastn and tblastx(Karlin et al., Proc. Natl. Acad. Sci. USA 87: 2264-2268 (1990) andAltschul, J. Mol. Evol. 36: 290-300 (1993), fully incorporated byreference) which are tailored for sequence similarity searching.

The approach used by the BLAST program is to first consider similarsegments between a query sequence and a database sequence, then toevaluate the statistical significance of all matches that are identifiedand finally to summarize only those matches which satisfy a preselectedthreshold of significance. For a discussion of basic issues insimilarity searching of sequence databases, see Altschul et al., (NatureGenetics 6: 119-129 (1994)) which is fully incorporated by reference.The search parameters for histogram, descriptions, alignments, expect(i.e., the statistical significance threshold for reporting matchesagainst database sequences), cutoff, matrix and filter are at thedefault settings. The default scoring matrix used by blastp, blastx,tblastn, and tblastx is the BLOSUM62 matrix (Henikoff et al., Proc.Natl. Acad. Sci. USA 89: 10915-10919 (1992), fully incorporated byreference). For blastn, the scoring matrix is set by the ratios of M(i.e., the reward score for a pair of matching residues) to N (i.e., thepenalty score for mismatching residues), wherein the default values forM and N are 5 and -4, respectively. Four blastn parameters may beadjusted as follows: Q=10 (gap creation penalty); R=10 (gap extensionpenalty); wink=1 (generates word hits at every wink^(th) position alongthe query); and gapw=16 (sets the window width within which gappedalignments are generated). The equivalent Blastp parameter settings wereQ=9; R=2; wink=1; and gapw=32. A Bestfit comparison between sequences,available in the GCG package version 10.0, uses DNA parameters GAP=50(gap creation penalty) and LEN=3 (gap extension penalty) and theequivalent settings in protein comparisons are GAP=8 and LEN=2.

The polynucleotide variants of the invention may contain alterations inthe coding regions, non-coding regions, or both. Especially preferredare polynucleotide variants containing alterations which produce silentsubstitutions, additions, or deletions, but do not alter the propertiesor activities of the encoded polypeptide. Nucleotide variants producedby silent substitutions due to the degeneracy of the genetic code arepreferred. Moreover, polypeptide variants in which less than 50, lessthan 40, less than 30, less than 20, less than 10, or 5-50, 5-25, 5-10,1-5, or 1-2 amino acids are substituted, deleted, or added in anycombination are also preferred. Polynucleotide variants can be producedfor a variety of reasons, e.g., to optimize codon expression for aparticular host (change codons in the human mRNA to those preferred by abacterial host, such as, yeast or E. coli).

In a preferred embodiment, a polynucleotide of the invention whichencodes the albumin portion of an albumin fusion protein is optimizedfor expression in yeast or mammalian cells. In a further preferredembodiment, a polynucleotide of the invention which encodes theTherapeutic protein portion of an albumin fusion protein is optimizedfor expression in yeast or mammalian cells. In a still further preferredembodiment, a polynucleotide encoding an albumin fusion protein of theinvention is optimized for expression in yeast or mammalian cells.

In an alternative embodiment, a codon optimized polynucleotide whichencodes a Therapeutic protein portion of an albumin fusion protein doesnot hybridize to the wild type polynucleotide encoding the Therapeuticprotein under stringent hybridization conditions as described herein. Ina further embodiment, a codon optimized polynucleotide which encodes analbumin portion of an albumin fusion protein does not hybridize to thewild type polynucleotide encoding the albumin protein under stringenthybridization conditions as described herein. In another embodiment, acodon optimized polynucleotide which encodes an albumin fusion proteindoes not hybridize to the wild type polynucleotide encoding theTherapeutic protein portion or the albumin protein portion understringent hybridization conditions as described herein.

In an additional embodiment, a polynucleotide which encodes aTherapeutic protein portion of an albumin fusion protein does notcomprise, or alternatively consist of, the naturally occurring sequenceof that Therapeutic protein. In a further embodiment, a polynucleotidewhich encodes an albumin protein portion of an albumin fusion proteindoes not comprise, or alternatively consist of, the naturally occurringsequence of albumin protein. In an alternative embodiment, apolynucleotide which encodes an albumin fusion protein does notcomprise, or alternatively consist of, the naturally occurring sequenceof a Therapeutic protein portion or the albumin protein portion.

Naturally occurring variants are called “allelic variants,” and refer toone of several alternate forms of a gene occupying a given locus on achromosome of an organism. (Genes II, Lewin, B., ed., John Wiley & Sons,New York (1985)). These allelic variants can vary at either thepolynucleotide and/or polypeptide level and are included in the presentinvention. Alternatively, non-naturally occurring variants may beproduced by mutagenesis techniques or by direct synthesis.

Using known methods of protein engineering and recombinant DNAtechnology, variants may be generated to improve or alter thecharacteristics of the polypeptides of the present invention. Forinstance, one or more amino acids can be deleted from the N-terminus orC-terminus of the polypeptide of the present invention withoutsubstantial loss of biological function. As an example, Ron et al. (J.Biol. Chem. 268: 2984-2988 (1993)) reported variant KGF proteins havingheparin binding activity even after deleting 3, 8, or 27 amino-terminalamino acid residues. Similarly, Interferon gamma exhibited up to tentimes higher activity after deleting 8-10 amino acid residues from thecarboxy terminus of this protein. (Dobeli et al., J. Biotechnology7:199-216 (1988).)

Moreover, ample evidence demonstrates that variants often retain abiological activity similar to that of the naturally occurring protein.For example, Gayle and coworkers (J. Biol. Chem. 268:22105-22111 (1993))conducted extensive mutational analysis of human cytokine IL-1a. Theyused random mutagenesis to generate over 3,500 individual IL-1a mutantsthat averaged 2.5 amino acid changes per variant over the entire lengthof the molecule. Multiple mutations were examined at every possibleamino acid position. The investigators found that “[m]ost of themolecule could be altered with little effect on either [binding orbiological activity].” In fact, only 23 unique amino acid sequences, outof more than 3,500 nucleotide sequences examined, produced a proteinthat significantly differed in activity from wild-type.

Furthermore, even if deleting one or more amino acids from theN-terminus or C-terminus of a polypeptide results in modification orloss of one or more biological functions, other biological activitiesmay still be retained. For example, the ability of a deletion variant toinduce and/or to bind antibodies which recognize the secreted form willlikely be retained when less than the majority of the residues of thesecreted form are removed from the N-terminus or C-terminus. Whether aparticular polypeptide lacking N- or C-terminal residues of a proteinretains such immunogenic activities can readily be determined by routinemethods described herein and otherwise known in the art.

Thus, the invention further includes polypeptide variants which have afunctional activity (e.g., biological activity and/or therapeuticactivity). In one embodiment, the invention provides variants of albuminfusion proteins that have a functional activity (e.g., biologicalactivity and/or therapeutic activity) that corresponds to one or morebiological and/or therapeutic activities of the Therapeutic proteincorresponding to the Therapeutic protein portion of the albumin fusionprotein. In another embodiment, the invention provides variants ofalbumin fusion proteins that have a functional activity (e.g.,biological activity and/or therapeutic activity) that corresponds to oneor more biological and/or therapeutic activities of the Therapeuticprotein corresponding to the Therapeutic protein portion of the albuminfusion protein. Such variants include deletions, insertions, inversions,repeats, and substitutions selected according to general rules known inthe art so as have little effect on activity. Polynucleotides encodingsuch variants are also encompassed by the invention.

In preferred embodiments, the variants of the invention haveconservative substitutions. By “conservative substitutions” is intendedswaps within groups such as replacement of the aliphatic or hydrophobicamino acids Ala, Val, Leu and Ile; replacement of the hydroxyl residuesSer and Thr; replacement of the acidic residues Asp and Glu; replacementof the amide residues Asn and Gln, replacement of the basic residuesLys, Arg, and His; replacement of the aromatic residues Phe, Tyr, andTrp, and replacement of the small-sized amino acids Ala, Ser, Thr, Met,and Gly.

Guidance concerning how to make phenotypically silent amino acidsubstitutions is provided, for example, in Bowie et al., “Decipheringthe Message in Protein Sequences: Tolerance to Amino AcidSubstitutions,” Science 247:1306-1310 (1990), wherein the authorsindicate that there are two main strategies for studying the toleranceof an amino acid sequence to change.

The first strategy exploits the tolerance of amino acid substitutions bynatural selection during the process of evolution. By comparing aminoacid sequences in different species, conserved amino acids can beidentified. These conserved amino acids are likely important for proteinfunction. In contrast, the amino acid positions where substitutions havebeen tolerated by natural selection indicates that these positions arenot critical for protein function. Thus, positions tolerating amino acidsubstitution could be modified while still maintaining biologicalactivity of the protein.

The second strategy uses genetic engineering to introduce amino acidchanges at specific positions of a cloned gene to identify regionscritical for protein function. For example, site directed mutagenesis oralanine-scanning mutagenesis (introduction of single alanine mutationsat every residue in the molecule) can be used. See Cunningham and Wells,Science 244:1081-1085 (1989). The resulting mutant molecules can then betested for biological activity.

As the authors state, these two strategies have revealed that proteinsare surprisingly tolerant of amino acid substitutions. The authorsfurther indicate which amino acid changes are likely to be permissive atcertain amino acid positions in the protein. For example, most buried(within the tertiary structure of the protein) amino acid residuesrequire nonpolar side chains, whereas few features of surface sidechains are generally conserved. Moreover, tolerated conservative aminoacid substitutions involve replacement of the aliphatic or hydrophobicamino acids Ala, Val, Leu and Ile; replacement of the hydroxyl residuesSer and Thr; replacement of the acidic residues Asp and Glu; replacementof the amide residues Asn and Gln, replacement of the basic residuesLys, Arg, and His; replacement of the aromatic residues Phe, Tyr, andTrp, and replacement of the small-sized amino acids Ala, Ser, Thr, Met,and Gly. Besides conservative amino acid substitution, variants of thepresent invention include (i) polypeptides containing substitutions ofone or more of the non-conserved amino acid residues, where thesubstituted amino acid residues may or may not be one encoded by thegenetic code, or (ii) polypeptides containing substitutions of one ormore of the amino acid residues having a substituent group, or (iii)polypeptides which have been fused with or chemically conjugated toanother compound, such as a compound to increase the stability and/orsolubility of the polypeptide (for example, polyethylene glycol), (iv)polypeptide containing additional amino acids, such as, for example, anIgG Fc fusion region peptide. Such variant polypeptides are deemed to bewithin the scope of those skilled in the art from the teachings herein.

For example, polypeptide variants containing amino acid substitutions ofcharged amino acids with other charged or neutral amino acids mayproduce proteins with improved characteristics, such as lessaggregation. Aggregation of pharmaceutical formulations both reducesactivity and increases clearance due to the aggregate's immunogenicactivity. See Pinckard et al., Clin. Exp. Immunol. 2:331-340 (1967);Robbins et al., Diabetes 36: 838-845 (1987); Cleland et al., Crit. Rev.Therapeutic Drug Carrier Systems 10:307-377 (1993).

In specific embodiments, the polypeptides of the invention comprise, oralternatively, consist of, fragments or variants of the amino acidsequence of an albumin fusion protein, the amino acid sequence of aTherapeutic protein and/or human serum albumin, wherein the fragments orvariants have 1-5, 5-10, 5-25, 5-50, 10-50 or 50-150, amino acid residueadditions, substitutions, and/or deletions when compared to thereference amino acid sequence. In preferred embodiments, the amino acidsubstitutions are conservative. Nucleic acids encoding thesepolypeptides are also encompassed by the invention.

The polypeptide of the present invention can be composed of amino acidsjoined to each other by peptide bonds or modified peptide bonds, i.e.,peptide isosteres, and may contain amino acids other than the 20gene-encoded amino acids. The polypeptides may be modified by eithernatural processes, such as post-translational processing, or by chemicalmodification techniques which are well known in the art. Suchmodifications are well described in basic texts and in more detailedmonographs, as well as in a voluminous research literature.Modifications can occur anywhere in a polypeptide, including the peptidebackbone, the amino acid side-chains and the amino or carboxyl termini.It will be appreciated that the same type of modification may be presentin the same or varying degrees at several sites in a given polypeptide.Also, a given polypeptide may contain many types of modifications.Polypeptides may be branched, for example, as a result ofubiquitination, and they may be cyclic, with or without branching.Cyclic, branched, and branched cyclic polypeptides may result fromposttranslation natural processes or may be made by synthetic methods.Modifications include acetylation, acylation, ADP-ribosylation,amidation, covalent attachment of flavin, covalent attachment of a hememoiety, covalent attachment of a nucleotide or nucleotide derivative,covalent attachment of a lipid or lipid derivative, covalent attachmentof phosphotidylinositol, cross-linking, cyclization, disulfide bondformation, demethylation, formation of covalent cross-links, formationof cysteine, formation of pyroglutamate, formylation,gamma-carboxylation, glycosylation, GPI anchor formation, hydroxylation,iodination, methylation, myristylation, oxidation, pegylation,proteolytic processing, phosphorylation, prenylation, racemization,selenoylation, sulfation, transfer-RNA mediated addition of amino acidsto proteins such as arginylation, and ubiquitination. (See, forinstance, PROTEINS—STRUCTURE AND MOLECULAR PROPERTIES, 2nd Ed., T. E.Creighton, W. H. Freeman and Company, New York (1993);POST-TRANSLATIONAL COVALENT MODIFICATION OF PROTEINS, B. C. Johnson,Ed., Academic Press, New York, pgs. 1-12 (1983); Seifter et al., Meth.Enzymol. 182:626-646 (1990); Rattan et al., Ann. N.Y. Acad. Sci.663:48-62 (1992)).

Functional Activity

“A polypeptide having functional activity” refers to a polypeptidecapable of displaying one or more known functional activities associatedwith the full-length, pro-protein, and/or mature form of a Therapeuticprotein. Such functional activities include, but are not limited to,biological activity, antigenicity [ability to bind (or compete with apolypeptide for binding) to an anti-polypeptide antibody],immunogenicity (ability to generate antibody which binds to a specificpolypeptide of the invention), ability to form multimers withpolypeptides of the invention, and ability to bind to a receptor orligand for a polypeptide.

“A polypeptide having biological activity” refers to a polypeptideexhibiting activity similar to, but not necessarily identical to, anactivity of a Therapeutic protein of the present invention, includingmature forms, as measured in a particular biological assay, with orwithout dose dependency. In the case where dose dependency does exist,it need not be identical to that of the polypeptide, but rathersubstantially similar to the dose-dependence in a given activity ascompared to the polypeptide of the present invention (i.e., thecandidate polypeptide will exhibit greater activity or not more thanabout 25-fold less and, preferably, not more than about tenfold lessactivity, and most preferably, not more than about three-fold lessactivity relative to the polypeptide of the present invention).

In preferred embodiments, an albumin fusion protein of the invention hasat least one biological and/or therapeutic activity associated with theTherapeutic protein portion (or fragment or variant thereof) when it isnot fused to albumin.

The albumin fusion proteins of the invention can be assayed forfunctional activity (e.g., biological activity) using or routinelymodifying assays known in the art, as well as assays described herein.Additionally, one of skill in the art may routinely assay fragments of aTherapeutic protein corresponding to a Therapeutic protein portion of analbumin fusion protein, for activity using assays referenced in itscorresponding row of Table 1 (e.g., in column 3 of Table 1). Further,one of skill in the art may routinely assay fragments of an albuminprotein corresponding to an albumin protein portion of an albumin fusionprotein, for activity using assays known in the art and/or as describedin the Examples section below.

For example, in one embodiment where one is assaying for the ability ofan albumin fusion protein to bind or compete with a Therapeutic proteinfor binding to an anti-Therapeutic polypeptide antibody and/oranti-albumin antibody, various immunoassays known in the art can beused, including but not limited to, competitive and non-competitiveassay systems using techniques such as radioimmunoassays, ELISA (enzymelinked immunosorbent assay), “sandwich” immunoassays, immunoradiometricassays, gel diffusion precipitation reactions, immunodiffusion assays,in situ immunoassays (using colloidal gold, enzyme or radioisotopelabels, for example), western blots, precipitation reactions,agglutination assays (e.g., gel agglutination assays, hemagglutinationassays), complement fixation assays, immunofluorescence assays, proteinA assays, and immunoelectrophoresis assays, etc. In one embodiment,antibody binding is detected by detecting a label on the primaryantibody. In another embodiment, the primary antibody is detected bydetecting binding of a secondary antibody or reagent to the primaryantibody. In a further embodiment, the secondary antibody is labeled.Many means are known in the art for detecting binding in an immunoassayand are within the scope of the present invention.

In a preferred embodiment, where a binding partner (e.g., a receptor ora ligand) of a Therapeutic protein is identified, binding to thatbinding partner by an albumin fusion protein which comprises thatTherapeutic protein as the Therapeutic protein portion of the fusion canbe assayed, e.g., by means well-known in the art, such as, for example,reducing and non-reducing gel chromatography, protein affinitychromatography, and affinity blotting. See generally, Phizicky et al.,Microbiol. Rev. 59:94-123 (1995). In another embodiment, the ability ofphysiological correlates of an albumin fusion protein to bind to asubstrate(s) of the Therapeutic polypeptide corresponding to theTherapeutic protein portion of the fusion can be routinely assayed usingtechniques known in the art.

In an alternative embodiment, where the ability of an albumin fusionprotein to multimerize is being evaluated, association with othercomponents of the multimer can be assayed, e.g., by means well-known inthe art, such as, for example, reducing and non-reducing gelchromatography, protein affinity chromatography, and affinity blotting.See generally, Phizicky et al., supra.

In preferred embodiments, an albumin fusion protein comprising all or aportion of an antibody that binds a Therapeutic protein, has at leastone biological and/or therapeutic activity (e.g., to specifically bind apolypeptide or epitope) associated with the antibody that binds aTherapeutic protein (or fragment or variant thereof) when it is notfused to albumin. In other preferred embodiments, the biologicalactivity and/or therapeutic activity of an albumin fusion proteincomprising all or a portion of an antibody that binds a Therapeuticprotein is the inhibition (i.e., antagonism) or activation (i.e.,agonism) of one or more of the biological activities and/or therapeuticactivities associated with the polypeptide that is specifically bound byantibody that binds a Therapeutic protein.

Albumin fusion proteins comprising at least a fragment or variant of anantibody that binds a Therapeutic protein may be characterized in avariety of ways. In particular, albumin fusion proteins comprising atleast a fragment or variant of an antibody that binds a Therapeuticprotein may be assayed for the ability to specifically bind to the sameantigens specifically bound by the antibody that binds a Therapeuticprotein corresponding to the Therapeutic protein portion of the albuminfusion protein using techniques described herein or routinely modifyingtechniques known in the art.

Assays for the ability of the albumin fusion proteins (e.g., comprisingat least a fragment or variant of an antibody that binds a Therapeuticprotein) to (specifically) bind a specific protein or epitope may beperformed in solution (e.g., Houghten, Bio/Techniques 13:412-421(1992)),on beads (e.g., Lam, Nature 354:82-84 (1991)), on chips (e.g., Fodor,Nature 364:555-556 (1993)), on bacteria (e.g., U.S. Pat. No. 5,223,409),on spores (e.g., U.S. Pat. Nos. 5,571,698; 5,403,484; and 5,223,409), onplasmids (e.g., Cull et al., Proc. Natl. Acad. Sci. USA 89:1865-1869(1992)) or on phage (e.g., Scott and Smith, Science 249:386-390 (1990);Devlin, Science 249:404-406 (1990); Cwirla et al., Proc. Natl. Acad.Sci. USA 87:6378-6382 (1990); and Felici, J. Mol. Biol. 222:301-310(1991)) (each of these references is incorporated herein in its entiretyby reference). Albumin fusion proteins comprising at least a fragment orvariant of a Therapeutic antibody may also be assayed for theirspecificity and affinity for a specific protein or epitope using orroutinely modifying techniques described herein or otherwise known inthe art.

The albumin fusion proteins comprising at least a fragment or variant ofan antibody that binds a Therapeutic protein may be assayed forcross-reactivity with other antigens (e.g., molecules that havesequence/structure conservation with the molecule(s) specifically boundby the antibody that binds a Therapeutic protein (or fragment or variantthereof) corresponding to the Therapeutic protein portion of the albuminfusion protein of the invention) by any method known in the art.

Immunoassays which can be used to analyze (immunospecific) binding andcross-reactivity include, but are not limited to, competitive andnon-competitive assay systems using techniques such as western blots,radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich”immunoassays, immunoprecipitation assays, precipitin reactions, geldiffusion precipitin reactions, immunodiffusion assays, agglutinationassays, complement-fixation assays, immunoradiometric assays,fluorescent immunoassays, and protein A immunoassays, to name but a few.Such assays are routine and well known in the art (see, e.g., Ausubel etal, eds, 1994, Current Protocols in Molecular Biology, Vol. 1, JohnWiley & Sons, Inc., New York, which is incorporated by reference hereinin its entirety). Exemplary immunoassays are described briefly below(but are not intended by way of limitation).

Immunoprecipitation protocols generally comprise lysing a population ofcells in a lysis buffer such as RIPA buffer (1% NP-40 or Triton X-100,1% sodium deoxycholate, 0.1% SDS, 0.15 M NaCl, 0.01 M sodium phosphateat pH 7.2, 1% Trasylol) supplemented with protein phosphatase and/orprotease inhibitors (e.g., EDTA, PMSF, aprotinin, sodium vanadate),adding the albumin fusion protein of the invention (e.g., comprising atleast a fragment or variant of an antibody that binds a Therapeuticprotein) to the cell lysate, incubating for a period of time (e.g., 1 to4 hours) at 40 degrees C., adding sepharose beads coupled to ananti-albumin antibody, for example, to the cell lysate, incubating forabout an hour or more at 40 degrees C., washing the beads in lysisbuffer and resuspending the beads in SDS/sample buffer. The ability ofthe albumin fusion protein to immunoprecipitate a particular antigen canbe assessed by, e.g., western blot analysis. One of skill in the artwould be knowledgeable as to the parameters that can be modified toincrease the binding of the albumin fusion protein to an antigen anddecrease the background (e.g., pre-clearing the cell lysate withsepharose beads). For further discussion regarding immunoprecipitationprotocols see, e.g., Ausubel et al, eds, 1994, Current Protocols inMolecular Biology, Vol. 1, John Wiley & Sons, Inc., New York at 10.16.1.

Western blot analysis generally comprises preparing protein samples,electrophoresis of the protein samples in a polyacrylamide gel (e.g.,8%-20% SDS-PAGE depending on the molecular weight of the antigen),transferring the protein sample from the polyacrylamide gel to amembrane such as nitrocellulose, PVDF or nylon, blocking the membrane inblocking solution (e.g., PBS with 3% BSA or non-fat milk), washing themembrane in washing buffer (e.g., PBS-Tween 20), applying the albuminfusion protein of the invention (diluted in blocking buffer) to themembrane, washing the membrane in washing buffer, applying a secondaryantibody (which recognizes the albumin fusion protein, e.g., ananti-human serum albumin antibody) conjugated to an enzymatic substrate(e.g., horseradish peroxidase or alkaline phosphatase) or radioactivemolecule (e.g., ³²P or ¹²⁵1) diluted in blocking buffer, washing themembrane in wash buffer, and detecting the presence of the antigen. Oneof skill in the art would be knowledgeable as to the parameters that canbe modified to increase the signal detected and to reduce the backgroundnoise. For further discussion regarding western blot protocols see,e.g., Ausubel et al, eds, 1994, Current Protocols in Molecular Biology,Vol. 1, John Wiley & Sons, Inc., New York at 10.8.1.

ELISAs comprise preparing antigen, coating the well of a 96-wellmicrotiter plate with the antigen, washing away antigen that did notbind the wells, adding the albumin fusion protein (e.g., comprising atleast a fragment or variant of an antibody that binds a Therapeuticprotein) of the invention conjugated to a detectable compound such as anenzymatic substrate (e.g., horseradish peroxidase or alkalinephosphatase) to the wells and incubating for a period of time, washingaway unbound or non-specifically bound albumin fusion proteins, anddetecting the presence of the albumin fusion proteins specifically boundto the antigen coating the well. In ELISAs the albumin fusion proteindoes not have to be conjugated to a detectable compound; instead, asecond antibody (which recognizes albumin fusion protein) conjugated toa detectable compound may be added to the well. Further, instead ofcoating the well with the antigen, the albumin fusion protein may becoated to the well. In this case, the detectable molecule could be theantigen conjugated to a detectable compound such as an enzymaticsubstrate (e.g., horseradish peroxidase or alkaline phosphatase). One ofskill in the art would be knowledgeable as to the parameters that can bemodified to increase the signal detected as well as other variations ofELISAs known in the art. For further discussion regarding ELISAs see,e.g., Ausubel et al, eds, 1994, Current Protocols in Molecular Biology,Vol. 1, John Wiley & Sons, Inc., New York at 11.2.1.

The binding affinity of an albumin fusion protein to a protein, antigen,or epitope and the off-rate of an albumin fusionprotein-protein/antigen/epitope interaction can be determined bycompetitive binding assays. One example of a competitive binding assayis a radioimmunoassay comprising the incubation of labeled antigen(e.g., ³H or ¹²⁵I) with the albumin fusion protein of the invention inthe presence of increasing amounts of unlabeled antigen, and thedetection of the antibody bound to the labeled antigen. The affinity ofthe albumin fusion protein for a specific protein, antigen, or epitopeand the binding off-rates can be determined from the data by Scatchardplot analysis. Competition with a second protein that binds the sameprotein, antigen or epitope as the albumin fusion protein, can also bedetermined using radioimmunoassays. In this case, the protein, antigenor epitope is incubated with an albumin fusion protein conjugated to alabeled compound (e.g., ³H or ¹²⁵I) in the presence of increasingamounts of an unlabeled second protein that binds the same protein,antigen, or epitope as the albumin fusion protein of the invention.

In a preferred embodiment, BIAcore kinetic analysis is used to determinethe binding on and off rates of albumin fusion proteins of the inventionto a protein, antigen or epitope. BIAcore kinetic analysis comprisesanalyzing the binding and dissociation of albumin fusion proteins, orspecific polypeptides, antigens or epitopes from chips with immobilizedspecific polypeptides, antigens or epitopes or albumin fusion proteins,respectively, on their surface.

Antibodies that bind a Therapeutic protein corresponding to theTherapeutic protein portion of an albumin fusion protein may also bedescribed or specified in terms of their binding affinity for a givenprotein or antigen, preferably the antigen which they specifically bind.Preferred binding affinities include those with a dissociation constantor Kd less than 5×10⁻² M, 10⁻² M, 5×10⁻³ M, 10⁻³ M, 5×10⁻⁴ M, 10⁻⁴ M.More preferred binding affinities include those with a dissociationconstant or Kd less than 5×10⁻⁵ M, 10⁻⁵ M, 5×10⁻⁶ M, 10⁻⁶M, 5×10⁻⁷ M,10⁷ M, 5×10⁻⁸ M or 10⁻⁸ M. Even more preferred binding affinitiesinclude those with a dissociation constant or Kd less than 5×10⁻⁹ M,10⁻⁹ M, 5×10⁻¹⁰ M, 10⁻¹⁰ M, 5×10⁻¹¹ M, 10⁻¹¹ M, 5×10⁻¹² M, ¹⁰⁻¹² M,5×10⁻¹³ M, 10⁻¹³ M, 5×10⁻¹⁴ M, 10⁻¹⁴ M, 5×10⁻¹⁵ M, or 10⁻¹⁵ M. Inpreferred embodiments, albumin fusion proteins comprising at least afragment or variant of an antibody that binds a Therapeutic protein, hasan affinity for a given protein or epitope similar to that of thecorresponding antibody (not fused to albumin) that binds a Therapeuticprotein, taking into account the valency of the albumin fusion protein(comprising at least a fragment or variant of an antibody that binds aTherapeutic protein) and the valency of the corresponding antibody. Inaddition, assays described herein (see Examples and Table 1) andotherwise known in the art may routinely be applied to measure theability of albumin fusion proteins and fragments, variants andderivatives thereof to elicit biological activity and/or Therapeuticactivity (either in vitro or in vivo) related to either the Therapeuticprotein portion and/or albumin portion of the albumin fusion protein.Other methods will be known to the skilled artisan and are within thescope of the invention.

Albumin

As described above, an albumin fusion protein of the invention comprisesat least a fragment or variant of a Therapeutic protein and at least afragment or variant of human serum albumin, which are associated withone another, preferably by genetic fusion.

An additional embodiment comprises at least a fragment or variant of aTherapeutic protein and at least a fragment or variant of human serumalbumin, which are linked to one another by chemical conjugation.

The terms, human serum albumin (HSA) and human albumin (HA) are usedinterchangeably herein. The terms, “albumin and “serum albumin” arebroader, and encompass human serum albumin (and fragments and variantsthereof) as well as albumin from other species (and fragments andvariants thereof).

As used herein, “albumin” refers collectively to albumin protein oramino acid sequence, or an albumin fragment or variant, having one ormore functional activities (e.g., biological activities) of albumin. Inparticular, “albumin” refers to human albumin or fragments thereof (seefor example, EP 201 239, EP 322 094 WO 97/24445, WO95/23857) especiallythe mature form of human albumin as shown in FIG. 1 and SEQ ID NO: 1038,or albumin from other vertebrates or fragments thereof, or analogs orvariants of these molecules or fragments thereof.

In preferred embodiments, the human serum albumin protein used in thealbumin fusion proteins of the invention contains one or both of thefollowing sets of point mutations with reference to SEQ ID NO: 1038:Leu-407 to Ala, Leu-408 to Val, Val-409 to Ala, and Arg-410 to Ala; orArg-410 to A, Lys-413 to Gln, and Lys-414 to Gln (see, e.g.,International Publication No. WO95/23857, hereby incorporated in itsentirety by reference herein). In even more preferred embodiments,albumin fusion proteins of the invention that contain one or both ofabove-described sets of point mutations have improvedstability/resistance to yeast Yap3p proteolytic cleavage, allowingincreased production of recombinant albumin fusion proteins expressed inyeast host cells.

As used herein, a portion of albumin sufficient to prolong thetherapeutic activity or shelf-life of the Therapeutic protein refers toa portion of albumin sufficient in length or structure to stabilize orprolong the therapeutic activity of the protein so that the shelf lifeof the Therapeutic protein portion of the albumin fusion protein isprolonged or extended compared to the shelf-life in the non-fusionstate. The albumin portion of the albumin fusion proteins may comprisethe full length of the HA sequence as described above, or may includeone or more fragments thereof that are capable of stabilizing orprolonging the therapeutic activity. Such fragments may be of 10 or moreamino acids in length or may include about 15, 20, 25, 30, 50, or morecontiguous amino acids from the HA sequence or may include part or allof specific domains of HA. For instance, one or more fragments of HAspanning the first two immunoglobulin-like domains may be used. In apreferred embodiment, the HA fragment is the mature form of HA.

The albumin portion of the albumin fusion proteins of the invention maybe a variant of normal HA. The Therapeutic protein portion of thealbumin fusion proteins of the invention may also be variants of theTherapeutic proteins as described herein. The term “variants” includesinsertions, deletions and substitutions, either conservative or nonconservative, where such changes do not substantially alter one or moreof the oncotic, useful ligand-binding and non-immunogenic properties ofalbumin, or the active site, or active domain which confers thetherapeutic activities of the Therapeutic proteins.

In particular, the albumin fusion proteins of the invention may includenaturally occurring polymorphic variants of human albumin and fragmentsof human albumin, for example those fragments disclosed in EP 322 094(namely HA (Pn), where n is 369 to 419). The albumin may be derived fromany vertebrate, especially any mammal, for example human, cow, sheep, orpig. Non-mammalian albumins include, but are not limited to, hen andsalmon. The albumin portion of the albumin fusion protein may be from adifferent animal than the Therapeutic protein portion.

Generally speaking, an HA fragment or variant will be at least 100 aminoacids long, preferably at least 150 amino acids long. The HA variant mayconsist of or alternatively comprise at least one whole domain of HA,for example domains 1 (amino acids 1-194 of SEQ ID NO: 1038), domain 2(amino acids 195-387 of SEQ ID NO: 1038), domain 3 (amino acids 388-585of SEQ ID NO: 1038), domains 1 and 2 (1-387 of SEQ ID NO: 1038), domains2 and 3 (195-585 of SEQ ID NO: 1038) or domains 1 and 3 (amino acids1-194 of SEQ ID NO: 1038 and amino acids 388-585 of SEQ ID NO: 1038).Each domain is itself made up of two homologous subdomains namely 1-105,120-194, 195-291, 316-387, 388-491 and 512-585, with flexibleinter-subdomain linker regions comprising residues Lys106 to Glu119,Glu292 to Val315 and Glu492 to Ala511.

Preferably, the albumin portion of an albumin fusion protein of theinvention comprises at least one subdomain or domain of HA orconservative modifications thereof. If the fusion is based onsubdomains, some or all of the adjacent linker is preferably used tolink to the Therapeutic protein moiety.

Antibodies that Specifically Bind Therapeutic Proteins are AlsoTherapeutic Proteins

The present invention also encompasses albumin fusion proteins thatcomprise at least a fragment or variant of an antibody that specificallybinds a Therapeutic protein disclosed in Table 1. It is specificallycontemplated that the term “Therapeutic protein” encompasses antibodiesthat bind a Therapeutic protein (e.g., as Described in column I ofTable 1) and fragments and variants thereof. Thus an albumin fusionprotein of the invention may contain at least a fragment or variant of aTherapeutic protein, and/or at least a fragment or variant of anantibody that binds a Therapeutic protein.

Antibody Structure and Background

The basic antibody structural unit is known to comprise a tetramer. Eachtetramer is composed of two identical pairs of polypeptide chains, eachpair having one “light” (about 25 kDa) and one “heavy” chain (about50-70 kDa). The amino-terminal portion of each chain includes a variableregion f about 100 to 110 or more amino acids primarily responsible forantigen recognition. The carboxy-terminal portion of each chain definesa constant region primarily responsible for effector function. Humanlight chains are classified as kappa and lambda light chains. Heavychains are classified as mu, delta, gamma, alpha, or epsilon, and definethe antibody's isotype as IgM, IgD, IgG, IgA, and IgE, respectively. Seegenerally, Fundamental Immunology Chapters 3-5 (Paul, W., ed., 4th ed.Raven Press, N.Y. (1998)) (incorporated by reference in its entirety forall purposes). The variable regions of each light/heavy chain pair formthe antibody binding site.

Thus, an intact IgG antibody has two binding sites. Except inbifunctional or bispecific antibodies, the two binding sites are thesame.

The chains all exhibit the same general structure of relativelyconserved framework regions (FR) joined by three hypervariable regions,also called complementarity determining regions or CDRs. The CDRregions, in general, are the portions of the antibody which make contactwith the antigen and determine its specificity. The CDRs from the heavyand the light chains of each pair are aligned by the framework regions,enabling binding to a specific epitope. From N-terminal to C-terminal,both light and heavy chains variable regions comprise the domains FR1,CDR1, FR2, CDR2, FR3, CDR3 and FR4. The variable regions are connectedto the heavy or light chain constant region. The assignment of aminoacids to each domain is in accordance with the definitions of KabatSequences of Proteins of Immunological Interest (National Institutes ofHealth, Bethesda, Md. (1987 and 1991)), or Chothia & Lesk J Mol. Biol.196:901-917 (1987); Chothia et al. Nature 342:878-883 (1989).

As used herein, “antibody” refers to immunoglobulin molecules andimmunologically active portions of immunoglobulin molecules, i.e.,molecules that contain an antigen binding site that specifically bindsan antigen (e.g., a molecule containing one or more CDR regions of anantibody). Antibodies that may correspond to a Therapeutic proteinportion of an albumin fusion protein include, but are not limited to,monoclonal, multispecific, human, humanized or chimeric antibodies,single chain antibodies (e.g., single chain Fvs), Fab fragments, F(ab′)fragments, fragments produced by a Fab expression library,anti-idiotypic (anti-Id) antibodies (including, e.g., anti-Id antibodiesspecific to antibodies of the invention), and epitope-binding fragmentsof any of the above (e.g., VH domains, VL domains, or one or more CDRregions).

Antibodies that Bind Therapeutic Proteins

The present invention encompasses albumin fusion proteins that compriseat least a fragment or variant of an antibody that binds a TherapeuticProtein (e.g., as disclosed in Table 1) or fragment or variant thereof.

Antibodies that bind a Therapeutic protein (or fragment or variantthereof) may be from any animal origin, including birds and mammals.Preferably, the antibodies are human, murine (e.g., mouse and rat),donkey, sheep, rabbit, goat, guinea pig, camel, horse, or chickenantibodies. Most preferably, the antibodies are human antibodies. Asused herein, “human” antibodies include antibodies having the amino acidsequence of a human immunoglobulin and include antibodies isolated fromhuman immunoglobulin libraries and xenomice or other organisms that havebeen genetically engineered to produce human antibodies.

The antibody molecules that bind to a Therapeutic protein and that maycorrespond to a Therapeutic protein portion of an albumin fusion proteinof the invention can be of any type (e.g., IgG, IgE, IgM, IgD, IgA andIgY), class (e.g., IgG1, IgG2, IgG3, IgG4, IgA1 and IgA2) or subclass ofimmunoglobulin molecule. In preferred embodiments, the antibodymolecules that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein are IgG1. Inother preferred embodiments, the immunoglobulin molecules that bind to aTherapeutic protein and that may correspond to a Therapeutic proteinportion of an albumin fusion protein are IgG2. In other preferredembodiments, the immunoglobulin molecules that bind to a Therapeuticprotein and that may correspond to a Therapeutic protein portion of analbumin fusion protein are IgG4.

Most preferably the antibodies that bind to a Therapeutic protein andthat may correspond to a Therapeutic protein portion of an albuminfusion protein are human antigen-binding antibody fragments of thepresent invention and include, but are not limited to, Fab, Fab′ andF(ab′)2, Fd, single-chain Fvs (scFv), single-chain antibodies,disulfide-linked Fvs (sdFv) and fragments comprising either a VL or VHdomain. Antigen-binding antibody fragments, including single-chainantibodies, may comprise the variable region(s) alone or in combinationwith the entirety or a portion of the following: hinge region, CH1, CH2,and CH3 domains.

The antibodies that bind to a Therapeutic protein and that maycorrespond to a Therapeutic protein portion of an albumin fusion proteinmay be monospecific, bispecific, trispecific or of greatermultispecificity. Multispecific antibodies may be specific for differentepitopes of a Therapeutic protein or may be specific for both aTherapeutic protein as well as for a heterologous epitope, such as aheterologous polypeptide or solid support material. See, e.g., PCTpublications WO 93/17715; WO 92/08802; WO 91/00360; WO 92/05793; Tutt,et al., J. Immunol. 147:60-69 (1991); U.S. Pat. Nos. 4,474,893;4,714,681; 4,925,648; 5,573,920; 5,601,819; Kostelny et al., J. Immunol.148:1547-1553 (1992).

Antibodies that bind a Therapeutic protein (or fragment or variantthereof) may be bispecific or bifunctional which means that the antibodyis an artificial hybrid antibody having two different heavy/light chainpairs and two different binding sites. Bispecific antibodies can beproduced by a variety of methods including fusion of hybridomas orlinking of Fab′ fragments. See, e.g., Songsivilai & Lachmann Clin. Exp.Immunol. 79: 315-321 (1990), Kostelny et al. J Immunol. 148:1547 1553(1992). In addition, bispecific antibodies may be formed as “diabodies”(Holliger et al. “‘Diabodies’: small bivalent and bispecific antibodyfragments” PNAS USA 90:6444-6448 (1993)) or “Janusins” (Traunecker etal. “Bispecific single chain molecules (Janusins) target cytotoxiclymphocytes on HIV infected cells” EMBO J 10:3655-3659 (1991) andTraunecker et al. “Janusin: new molecular design for bispecificreagents” Int J Cancer Suppl 7:51-52 (1992)).

The present invention also provides albumin fusion proteins thatcomprise, fragments or variants (including derivatives) of an antibodydescribed herein or known elsewhere in the art. Standard techniquesknown to those of skill in the art can be used to introduce mutations inthe nucleotide sequence encoding a molecule of the invention, including,for example, site-directed mutagenesis and PCR-mediated mutagenesiswhich result in amino acid substitutions. Preferably, the variants(including derivatives) encode less than 50 amino acid substitutions,less than 40 amino acid substitutions, less than 30 amino acidsubstitutions, less than 25 amino acid substitutions, less than 20 aminoacid substitutions, less than 15 amino acid substitutions, less than 10amino acid substitutions, less than 5 amino acid substitutions, lessthan 4 amino acid substitutions, less than 3 amino acid substitutions,or less than 2 amino acid substitutions relative to the reference VHdomain, VHCDR1, VHCDR2, VHCDR3, VL domain, VLCDR1, VLCDR2, or VLCDR3. Inspecific embodiments, the variants encode substitutions of VHCDR3. In apreferred embodiment, the variants have conservative amino acidsubstitutions at one or more predicted non-essential amino acidresidues.

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein may bedescribed or specified in terms of the epitope(s) or portion(s) of aTherapeutic protein which they recognize or specifically bind.Antibodies which specifically bind a Therapeutic protein or a specificepitope of a Therapeutic protein may also be excluded. Therefore, thepresent invention encompasses antibodies that specifically bindTherapeutic proteins, and allows for the exclusion of the same. Inpreferred embodiments, albumin fusion proteins comprising at least afragment or variant of an antibody that binds a Therapeutic protein,binds the same epitopes as the unfused fragment or variant of thatantibody itself.

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein may also bedescribed or specified in terms of their cross-reactivity. Antibodiesthat do not bind any other analog, ortholog, or homolog of a Therapeuticprotein are included. Antibodies that bind polypeptides with at least95%, at least 90%, at least 85%, at least 80%, at least 75%, at least70%, at least 65%, at least 60%, at least 55%, and at least 50% sequenceidentity (as calculated using methods known in the art and describedherein) to a Therapeutic protein are also included in the presentinvention. In specific embodiments, antibodies that bind to aTherapeutic protein and that may correspond to a Therapeutic proteinportion of an albumin fusion protein cross-react with murine, rat and/orrabbit homologs of human proteins and the corresponding epitopesthereof. Antibodies that do not bind polypeptides with less than 95%,less than 90%, less than 85%, less than 80%, less than 75%, less than70%, less than 65%, less than 60%, less than 55%, and less than 50%sequence identity (as calculated using methods known in the art anddescribed herein) to a Therapeutic protein are also included in thepresent invention. In a specific embodiment, the above-describedcross-reactivity is with respect to any single specific antigenic orimmunogenic polypeptide, or combination(s) of 2, 3, 4, 5, or more of thespecific antigenic and/or immunogenic polypeptides disclosed herein. Inpreferred embodiments, albumin fusion proteins comprising at least afragment or variant of an antibody that binds a Therapeutic protein, hassimilar or substantially identical cross reactivity characteristicscompared to the fragment or variant of that particular antibody itself.

Further included in the present invention are antibodies which bindpolypeptides encoded by polynucleotides which hybridize to apolynucleotide encoding a Therapeutic protein under stringenthybridization conditions (as described herein). Antibodies that bind toa Therapeutic protein and that may correspond to a Therapeutic proteinportion of an albumin fusion protein of the invention may also bedescribed or specified in terms of their binding affinity to apolypeptide of the invention. Preferred binding affinities include thosewith a dissociation constant or Kd less than 5×10⁻² M, 10⁻² M, 5×10⁻³ M,10⁻³ M, 5×10⁻⁴ M, 10⁻⁴ M. More preferred binding affinities includethose with a dissociation constant or Kd less than 5×10⁻⁵ M, 10⁻⁵ M,5×10⁻⁶ M, 10⁻⁶M, 5×10⁻⁷ M, 10⁷ M, 5×10⁻⁸ M or 10⁻⁸ M. Even morepreferred binding affinities include those with a dissociation constantor Kd less than 5×10⁻⁹ M, 10⁻⁹ M, 5×10⁻¹⁰ M, 10⁻¹⁰ M, 5×10⁻¹¹ M, 10⁻¹¹M, 5×10⁻¹² M, ¹⁰⁻¹² M, 5×10⁻¹³ M, 10⁻¹³ M, 5×10⁻¹⁴ M, 10⁻¹⁴ M, 5×10⁻¹⁵M, or 10⁻¹⁵ M. In preferred embodiments, albumin fusion proteinscomprising at least a fragment or variant of an antibody that binds aTherapeutic protein, has an affinity for a given protein or epitopesimilar to that of the corresponding antibody (not fused to albumin)that binds a Therapeutic protein, taking into account the valency of thealbumin fusion protein (comprising at least a fragment or variant of anantibody that binds a Therapeutic protein) and the valency of thecorresponding antibody.

The invention also provides antibodies that competitively inhibitbinding of an antibody to an epitope of a Therapeutic protein asdetermined by any method known in the art for determining competitivebinding, for example, the immunoassays described herein. In preferredembodiments, the antibody competitively inhibits binding to the epitopeby at least 95%, at least 90%, at least 85%, at least 80%, at least 75%,at least 70%, at least 60%, or at least 50%. In preferred embodiments,albumin fusion proteins comprising at least a fragment or variant of anantibody that binds a Therapeutic protein, competitively inhibitsbinding of a second antibody to an epitope of a Therapeutic protein. Inother preferred embodiments, albumin fusion proteins comprising at leasta fragment or variant of an antibody that binds a Therapeutic protein,competitively inhibits binding of a second antibody to an epitope of aTherapeutic protein by at least 95%, at least 90%, at least 85%, atleast 80%, at least 75%, at least 70%, at least 60%, or at least 50%.

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein of theinvention may act as agonists or antagonists of the Therapeutic protein.For example, the present invention includes antibodies which disrupt thereceptor/ligand interactions with the polypeptides of the inventioneither partially or fully. The invention features both receptor-specificantibodies and ligand-specific antibodies. The invention also featuresreceptor-specific antibodies which do not prevent ligand binding butprevent receptor activation. Receptor activation (i.e., signaling) maybe determined by techniques described herein or otherwise known in theart. For example, receptor activation can be determined by detecting thephosphorylation (e.g., tyrosine or serine/threonine) of the receptor orits substrate by immunoprecipitation followed by western blot analysis(for example, as described supra). In specific embodiments, antibodiesare provided that inhibit ligand activity or receptor activity by atleast 95%, at least 90%, at least 85%, at least 80%, at least 75%, atleast 70%, at least 60%, or at least 50% of the activity in absence ofthe antibody. In preferred embodiments, albumin fusion proteinscomprising at least a fragment or variant of an antibody that binds aTherapeutic protein, has similar or substantially similarcharacteristics with regard to preventing ligand binding and/orpreventing receptor activation compared to an un-fused fragment orvariant of the antibody that binds the Therapeutic protein.

The invention also features receptor-specific antibodies which bothprevent ligand binding and receptor activation as well as antibodiesthat recognize the receptor-ligand complex, and, preferably, do notspecifically recognize the unbound receptor or the unbound ligand.Likewise, included in the invention are neutralizing antibodies whichbind the ligand and prevent binding of the ligand to the receptor, aswell as antibodies which bind the ligand, thereby preventing receptoractivation, but do not prevent the ligand from binding the receptor.Further included in the invention are antibodies which activate thereceptor. These antibodies may act as receptor agonists, i.e.,potentiate or activate either all or a subset of the biologicalactivities of the ligand-mediated receptor activation, for example, byinducing dimerization of the receptor. The antibodies may be specifiedas agonists, antagonists or inverse agonists for biological activitiescomprising the specific biological activities of the Therapeuticproteins (e.g. as disclosed in Table 1). The above antibody agonists canbe made using methods known in the art. See, e.g., PCT publication WO96/40281; U.S. Pat. No. 5,811,097; Deng et al., Blood 92(6):1981-1988(1998); Chen et al., Cancer Res. 58(16):3668-3678 (1998); Harrop et al.,J. Immunol. 161(4):1786-1794 (1998); Zhu et al., Cancer Res.58(15):3209-3214 (1998); Yoon et al., J. Immunol. 160(7):3170-3179(1998); Prat et al., J. Cell. Sci. 111(Pt2):237-247 (1998); Pitard etal., J. Immunol. Methods 205(2):177-190 (1997); Liautard et al.,Cytokine 9(4):233-241 (1997); Carlson et al., J. Biol. Chem.272(17):11295-11301 (1997); Taryman et al., Neuron 14(4):755-762 (1995);Muller et al., Structure 6(9):1153-1167 (1998); Bartunek et al.,Cytokine 8(1):14-20 (1996) (which are all incorporated by referenceherein in their entireties). In preferred embodiments, albumin fusionproteins comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein, have similar or substantially identicalagonist or antagonist properties as an un-fused fragment or variant ofthe antibody that binds the Therapeutic protein.

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein of theinvention may be used, for example, to purify, detect, and targetTherapeutic proteins, including both in in vitro and in vivo diagnosticand therapeutic methods. For example, the antibodies have utility inimmunoassays for qualitatively and quantitatively measuring levels ofthe Therapeutic protein in biological samples. See, e.g., Harlow et al.,Antibodies: A Laboratory Manual, (Cold Spring Harbor Laboratory Press,2nd ed. 1988); incorporated by reference herein in its entirety.Likewise, albumin fusion proteins comprising at least a fragment orvariant of an antibody that binds a Therapeutic protein, may be used,for example, to purify, detect, and target Therapeutic proteins,including both in vitro and in vivo diagnostic and therapeutic methods.

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein includederivatives that are modified, i.e., by the covalent attachment of anytype of molecule to the antibody. For example, but not by way oflimitation, the antibody derivatives include antibodies that have beenmodified, e.g., by glycosylation, acetylation, pegylation,phosphorylation, amidation, derivatization by known protecting/blockinggroups, proteolytic cleavage, linkage to a cellular ligand or otherprotein, etc. Any of numerous chemical modifications may be carried outby known techniques, including, but not limited to specific chemicalcleavage, acetylation, formylation, metabolic synthesis of tunicamycin,etc. Additionally, the derivative may contain one or more non-classicalamino acids. Albumin fusion proteins of the invention may also bemodified as described above.

Methods of Producing Antibodies that Bind Therapeutic Proteins

The antibodies that bind to a Therapeutic protein and that maycorrespond to a Therapeutic protein portion of an albumin fusion proteinof the invention may be generated by any suitable method known in theart. Polyclonal antibodies to an antigen-of-interest can be produced byvarious procedures well known in the art. For example, a Therapeuticprotein may be administered to various host animals including, but notlimited to, rabbits, mice, rats, etc. to induce the production of seracontaining polyclonal antibodies specific for the antigen. Variousadjuvants may be used to increase the immunological response, dependingon the host species, and include but are not limited to, Freund's(complete and incomplete), mineral gels such as aluminum hydroxide,surface active substances such as lysolecithin, pluronic polyols,polyanions, peptides, oil emulsions, keyhole limpet hemocyanins,dinitrophenol, and potentially useful human adjuvants such as BCG(bacille Calmette-Guerin) and corynebacterium parvum. Such adjuvants arealso well known in the art.

Monoclonal antibodies can be prepared using a wide variety of techniquesknown in the art including the use of hybridoma, recombinant, and phagedisplay technologies, or a combination thereof. For example, monoclonalantibodies can be produced using hybridoma techniques including thoseknown in the art and taught, for example, in Harlow et al., Antibodies:A Laboratory Manual, (Cold Spring Harbor Laboratory Press, 2nd ed.1988); Hammerling, et al., in: Monoclonal Antibodies and T-CellHybridomas 563-681 (Elsevier, N. Y., 1981) (said references incorporatedby reference in their entireties). The term “monoclonal antibody” asused herein is not limited to antibodies produced through hybridomatechnology. The term “monoclonal antibody” refers to an antibody that isderived from a single clone, including any eukaryotic, prokaryotic, orphage clone, and not the method by which it is produced.

Methods for producing and screening for specific antibodies usinghybridoma technology are routine and well known in the art. In anon-limiting example, mice can be immunized with a Therapeutic proteinor fragment or variant thereof, an albumin fusion protein, or a cellexpressing such a Therapeutic protein or fragment or variant thereof oralbumin fusion protein. Once an immune response is detected, e.g.,antibodies specific for the antigen are detected in the mouse serum, themouse spleen is harvested and splenocytes isolated. The splenocytes arethen fused by well known techniques to any suitable myeloma cells, forexample cells from cell line SP20 available from the ATCC. Hybridomasare selected and cloned by limited dilution. The hybridoma clones arethen assayed by methods known in the art for cells that secreteantibodies capable of binding a polypeptide of the invention. Ascitesfluid, which generally contains high levels of antibodies, can begenerated by immunizing mice with positive hybridoma clones.

Accordingly, the present invention provides methods of generatingmonoclonal antibodies as well as antibodies produced by the methodcomprising culturing a hybridoma cell secreting an antibody wherein,preferably, the hybridoma is generated by fusing splenocytes isolatedfrom a mouse immunized with an antigen of the invention with myelomacells and then screening the hybridomas resulting from the fusion forhybridoma clones that secrete an antibody able to bind a polypeptide ofthe invention.

Another well known method for producing both polyclonal and monoclonalhuman B cell lines is transformation using Epstein Barr Virus (EBV).Protocols for generating EBV-transformed B cell lines are commonly knownin the art, such as, for example, the protocol outlined in Chapter 7.22of Current Protocols in Immunology, Coligan et al., Eds., 1994, JohnWiley & Sons, NY, which is hereby incorporated in its entirety byreference. The source of B cells for transformation is commonly humanperipheral blood, but B cells for transformation may also be derivedfrom other sources including, but not limited to, lymph nodes, tonsil,spleen, tumor tissue, and infected tissues. Tissues are generally madeinto single cell suspensions prior to EBV transformation. Additionally,steps may be taken to either physically remove or inactivate T cells(e.g., by treatment with cyclosporin A) in B cell-containing samples,because T cells from individuals seropositive for anti-EBV antibodiescan suppress B cell immortalization by EBV.

In general, the sample containing human B cells is innoculated with EBV,and cultured for 3-4 weeks. A typical source of EBV is the culturesupernatant of the B95-8 cell line (ATCC #VR-1492). Physical signs ofEBV transformation can generally be seen towards the end of the 3-4 weekculture period. By phase-contrast microscopy, transformed cells mayappear large, clear, hairy and tend to aggregate in tight clusters ofcells. Initially, EBV lines are generally polyclonal. However, overprolonged periods of cell cultures, EBV lines may become monoclonal orpolyclonal as a result of the selective outgrowth of particular B cellclones. Alternatively, polyclonal EBV transformed lines may be subcloned(e.g., by limiting dilution culture) or fused with a suitable fusionpartner and plated at limiting dilution to obtain monoclonal B celllines. Suitable fusion partners for EBV transformed cell lines includemouse myeloma cell lines (e.g., SP2/0, X63-Ag8.653), heteromyeloma celllines (human x mouse; e.g, SPAM-8, SBC-H20, and CB-F7), and human celllines (e.g., GM 1500, SKO-007, RPMI 8226, and KR-4). Thus, the presentinvention also provides a method of generating polyclonal or monoclonalhuman antibodies against polypeptides of the invention or fragmentsthereof, comprising EBV-transformation of human B cells.

Antibody fragments which recognize specific epitopes may be generated byknown techniques. For example, Fab and F(ab′)2 fragments of theinvention may be produced by proteolytic cleavage of immunoglobulinmolecules, using enzymes such as papain (to produce Fab fragments) orpepsin (to produce F(ab′)2 fragments). F(ab′)2 fragments contain thevariable region, the light chain constant region and the CH1 domain ofthe heavy chain.

For example, antibodies that bind to a Therapeutic protein can also begenerated using various phage display methods known in the art. In phagedisplay methods, functional antibody domains are displayed on thesurface of phage particles which carry the polynucleotide sequencesencoding them. In a particular embodiment, such phage can be utilized todisplay antigen binding domains expressed from a repertoire orcombinatorial antibody library (e.g., human or murine). Phage expressingan antigen binding domain that binds the antigen of interest can beselected or identified with antigen, e.g., using labeled antigen orantigen bound or captured to a solid surface or bead. Phage used inthese methods are typically filamentous phage including fd and M13binding domains expressed from phage with Fab, Fv or disulfidestabilized Fv antibody domains recombinantly fused to either the phagegene III or gene VIII protein. Examples of phage display methods thatcan be used to make antibodies that bind to a Therapeutic proteininclude those disclosed in Brinkman et al., J. Immunol. Methods182:41-50 (1995); Ames et al., J. Immunol. Methods 184:177-186 (1995);Kettleborough et al., Eur. J. Immunol. 24:952-958 (1994); Persic et al.,Gene 187 9-18 (1997); Burton et al., Advances in Immunology 57:191-280(1994); PCT application No. PCT/GB91/01134; PCT publications WO90/02809; WO 91/10737; WO 92/01047; WO 92/18619; WO 93/11236; WO95/15982; WO 95/20401; and U.S. Pat. Nos. 5,698,426; 5,223,409;5,403,484; 5,580,717; 5,427,908; 5,750,753; 5,821,047; 5,571,698;5,427,908; 5,516,637; 5,780,225; 5,658,727; 5,733,743 and 5,969,108;each of which is incorporated herein by reference in its entirety.

As described in the above references, after phage selection, theantibody coding regions from the phage can be isolated and used togenerate whole antibodies, including human antibodies, or any otherdesired antigen binding fragment, and expressed in any desired host,including mammalian cells, insect cells, plant cells, yeast, andbacteria, e.g., as described in detail below. For example, techniques torecombinantly produce Fab, Fab′ and F(ab′)2 fragments can also beemployed using methods known in the art such as those disclosed in PCTpublication WO 92/22324; Mullinax et al., BioTechniques 12(6):864-869(1992); and Sawai et al., AJRI 34:26-34 (1995); and Better et al.,Science 240:1041-1043 (1988) (said references incorporated by referencein their entireties).

Examples of techniques which can be used to produce single-chain Fvs andantibodies include those described in U.S. Pat. Nos. 4,946,778 and5,258,498; Huston et al., Methods in Enzymology 203:46-88 (1991); Shu etal., PNAS 90:7995-7999 (1993); and Skerra et al., Science 240:1038-1040(1988). For some uses, including in vivo use of antibodies in humans andin vitro detection assays, it may be preferable to use chimeric,humanized, or human antibodies. A chimeric antibody is a molecule inwhich different portions of the antibody are derived from differentanimal species, such as antibodies having a variable region derived froma murine monoclonal antibody and a human immunoglobulin constant region.Methods for producing chimeric antibodies are known in the art. Seee.g., Morrison, Science 229:1202 (1985); Oi et al., BioTechniques 4:214(1986); Gillies et al., (1989) J. Immunol. Methods 125:191-202; U.S.Pat. Nos. 5,807,715; 4,816,567; and 4,816397, which are incorporatedherein by reference in their entirety. Humanized antibodies are antibodymolecules from non-human species antibody that binds the desired antigenhaving one or more complementarity determining regions (CDRs) from thenon-human species and a framework regions from a human immunoglobulinmolecule. Often, framework residues in the human framework regions willbe substituted with the corresponding residue from the CDR donorantibody to alter, preferably improve, antigen binding. These frameworksubstitutions are identified by methods well known in the art, e.g., bymodeling of the interactions of the CDR and framework residues toidentify framework residues important for antigen binding and sequencecomparison to identify unusual framework residues at particularpositions. (See, e.g., Queen et al., U.S. Pat. No. 5,585,089; Riechmannet al., Nature 332:323 (1988), which are incorporated herein byreference in their entireties.) Antibodies can be humanized using avariety of techniques known in the art including, for example,CDR-grafting (EP 239,400; PCT publication WO 91/09967; U.S. Pat. Nos.5,225,539; 5,530,101; and 5,585,089), veneering or resurfacing (EP592,106; EP 519,596; Padlan, Molecular Immunology 28(4/5):489-498(1991); Studnicka et al., Protein Engineering 7(6):805-814 (1994);Roguska. et al., PNAS 91:969-973 (1994)), and chain shuffling (U.S. Pat.No. 5,565,332).

Completely human antibodies are particularly desirable for therapeutictreatment of human patients. Human antibodies can be made by a varietyof methods known in the art including phage display methods describedabove using antibody libraries derived from human immunoglobulinsequences. See also, U.S. Pat. Nos. 4,444,887 and 4,716,111; and PCTpublications WO 98/46645, WO 98/50433, WO 98/24893, WO 98/16654, WO96/34096, WO 96/33735, and WO 91/10741; each of which is incorporatedherein by reference in its entirety.

Human antibodies can also be produced using transgenic mice which areincapable of expressing functional endogenous immunoglobulins, but whichcan express human immunoglobulin genes. For example, the human heavy andlight chain immunoglobulin gene complexes may be introduced randomly orby homologous recombination into mouse embryonic stem cells.Alternatively, the human variable region, constant region, and diversityregion may be introduced into mouse embryonic stem cells in addition tothe human heavy and light chain genes. The mouse heavy and light chainimmunoglobulin genes may be rendered non-functional separately orsimultaneously with the introduction of human immunoglobulin loci byhomologous recombination. In particular, homozygous deletion of the JHregion prevents endogenous antibody production. The modified embryonicstem cells are expanded and microinjected into blastocysts to producechimeric mice. The chimeric mice are then bred to produce homozygousoffspring which express human antibodies. The transgenic mice areimmunized in the normal fashion with a selected antigen, e.g., all or aportion of a polypeptide of the invention. Monoclonal antibodiesdirected against the antigen can be obtained from the immunized,transgenic mice using conventional hybridoma technology. The humanimmunoglobulin transgenes harbored by the transgenic mice rearrangeduring B cell differentiation, and subsequently undergo class switchingand somatic mutation. Thus, using such a technique, it is possible toproduce therapeutically useful IgG, IgA, IgM and IgE antibodies. For anoverview of this technology for producing human antibodies, see Lonbergand Huszar, Int. Rev. Immunol. 13:65-93 (1995). For a detaileddiscussion of this technology for producing human antibodies and humanmonoclonal antibodies and protocols for producing such antibodies, see,e.g., PCT publications WO 98/24893; WO 92/01047; WO 96/34096; WO96/33735; European Patent No. 0 598 877; U.S. Pat. Nos. 5,413,923;5,625,126; 5,633,425; 5,569,825; 5,661,016; 5,545,806; 5,814,318;5,885,793; 5,916,771; 5,939,598; 6,075,181; and 6,114,598, which areincorporated by reference herein in their entirety. In addition,companies such as Abgenix, Inc. (Freemont, Calif.) and Genpharm (SanJose, Calif.) can be engaged to provide human antibodies directedagainst a selected antigen using technology similar to that describedabove.

Completely human antibodies which recognize a selected epitope can begenerated using a technique referred to as “guided selection.” In thisapproach a selected non-human monoclonal antibody, e.g., a mouseantibody, is used to guide the selection of a completely human antibodyrecognizing the same epitope. (Jespers et al., Bio/technology 12:899-903(1988)).

Polynucleotides Encoding Antibodies

The invention further provides polynucleotides comprising a nucleotidesequence encoding an antibody and fragments thereof. The invention alsoencompasses polynucleotides that hybridize under stringent oralternatively, under lower stringency hybridization conditions, e.g., asdefined supra, to polynucleotides that encode an antibody, preferably,that specifically binds to a Therapeutic protein, and more preferably,an antibody that binds to a polypeptide having the amino acid sequenceof a “Therapeutic protein:X” as disclosed in the “SEQ ID NO:Z” column ofTable 2.

The polynucleotides may be obtained, and the nucleotide sequence of thepolynucleotides determined, by any method known in the art. For example,if the nucleotide sequence of the antibody is known, a polynucleotideencoding the antibody may be assembled from chemically synthesizedoligonucleotides (e.g., as described in Kutmeier et al., BioTechniques17:242 (1994)), which, briefly, involves the synthesis of overlappingoligonucleotides containing portions of the sequence encoding theantibody, annealing and ligating of those oligonucleotides, and thenamplification of the ligated oligonucleotides by PCR.

Alternatively, a polynucleotide encoding an antibody may be generatedfrom nucleic acid from a suitable source. If a clone containing anucleic acid encoding a particular antibody is not available, but thesequence of the antibody molecule is known, a nucleic acid encoding theimmunoglobulin may be chemically synthesized or obtained from a suitablesource (e.g., an antibody cDNA library, or a cDNA library generatedfrom, or nucleic acid, preferably poly A+RNA, isolated from, any tissueor cells expressing the antibody, such as hybridoma cells selected toexpress an antibody) by PCR amplification using synthetic primershybridizable to the 3′ and 5′ ends of the sequence or by cloning usingan oligonucleotide probe specific for the particular gene sequence toidentify, e.g., a cDNA clone from a cDNA library that encodes theantibody. Amplified nucleic acids generated by PCR may then be clonedinto replicable cloning vectors using any method well known in the art(See Example 107).

Once the nucleotide sequence and corresponding amino acid sequence ofthe antibody is determined, the nucleotide sequence of the antibody maybe manipulated using methods well known in the art for the manipulationof nucleotide sequences, e.g., recombinant DNA techniques, site directedmutagenesis, PCR, etc. (see, for example, the techniques described inSambrook et al., 1990, Molecular Cloning, A Laboratory Manual, 2d Ed.,Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. and Ausubel etal., eds., 1998, Current Protocols in Molecular Biology, John Wiley &Sons, NY, which are both incorporated by reference herein in theirentireties), to generate antibodies having a different amino acidsequence, for example to create amino acid substitutions, deletions,and/or insertions.

In a specific embodiment, the amino acid sequence of the heavy and/orlight chain variable domains may be inspected to identify the sequencesof the complementarity determining regions (CDRs) by methods that arewell know in the art, e.g., by comparison to known amino acid sequencesof other heavy and light chain variable regions to determine the regionsof sequence hypervariability. Using routine recombinant DNA techniques,one or more of the CDRs may be inserted within framework regions, e.g.,into human framework regions to humanize a non-human antibody, asdescribed supra. The framework regions may be naturally occurring orconsensus framework regions, and preferably human framework regions(see, e.g., Chothia et al., J. Mol. Biol. 278: 457-479 (1998) for alisting of human framework regions). Preferably, the polynucleotidegenerated by the combination of the framework regions and CDRs encodesan antibody that specifically binds a polypeptide of the invention.Preferably, as discussed supra, one or more amino acid substitutions maybe made within the framework regions, and, preferably, the amino acidsubstitutions improve binding of the antibody to its antigen.Additionally, such methods may be used to make amino acid substitutionsor deletions of one or more variable region cysteine residuesparticipating in an intrachain disulfide bond to generate antibodymolecules lacking one or more intrachain disulfide bonds. Otheralterations to the polynucleotide are encompassed by the presentinvention and within the skill of the art.

In addition, techniques developed for the production of “chimericantibodies” (Morrison et al., Proc. Natl. Acad. Sci. 81:851-855 (1984);Neuberger et al., Nature 312:604-608 (1984); Takeda et al., Nature314:452-454 (1985)) by splicing genes from a mouse antibody molecule ofappropriate antigen specificity together with genes from a humanantibody molecule of appropriate biological activity can be used. Asdescribed supra, a chimeric antibody is a molecule in which differentportions are derived from different animal species, such as those havinga variable region derived from a murine mAb and a human immunoglobulinconstant region, e.g., humanized antibodies.

Alternatively, techniques described for the production of single chainantibodies (U.S. Pat. No. 4,946,778; Bird, Science 242:423-42 (1988);Huston et al., Proc. Natl. Acad. Sci. USA 85:5879-5883 (1988); and Wardet al., Nature 334:544-54 (1989)) can be adapted to produce single chainantibodies. Single chain antibodies are formed by linking the heavy andlight chain fragments of the Fv region via an amino acid bridge,resulting in a single chain polypeptide. Techniques for the assembly offunctional Fv fragments in E. coli may also be used (Skerra et al.,Science 242:1038-1041 (1988)).

Recombinant Expression of Antibodies

Recombinant expression of an antibody, or fragment, derivative or analogthereof, (e.g., a heavy or light chain of an antibody or a single chainantibody), requires construction of an expression vector containing apolynucleotide that encodes the antibody. Once a polynucleotide encodingan antibody molecule or a heavy or light chain of an antibody, orportion thereof (preferably containing the heavy or light chain variabledomain), of the invention has been obtained, the vector for theproduction of the antibody molecule may be produced by recombinant DNAtechnology using techniques well known in the art. Thus, methods forpreparing a protein by expressing a polynucleotide containing anantibody encoding nucleotide sequence are described herein. Methodswhich are well known to those skilled in the art can be used toconstruct expression vectors containing antibody coding sequences andappropriate transcriptional and translational control signals. Thesemethods include, for example, in vitro recombinant DNA techniques,synthetic techniques, and in vivo genetic recombination. The invention,thus, provides replicable vectors comprising a nucleotide sequenceencoding an antibody molecule of the invention, or a heavy or lightchain thereof, or a heavy or light chain variable domain, operablylinked to a promoter. Such vectors may include the nucleotide sequenceencoding the constant region of the antibody molecule (see, e.g., PCTPublication WO 86/05807; PCT Publication WO 89/01036; and U.S. Pat. No.5,122,464) and the variable domain of the antibody may be cloned intosuch a vector for expression of the entire heavy or light chain.

The expression vector is transferred to a host cell by conventionaltechniques and the transfected cells are then cultured by conventionaltechniques to produce an antibody. Thus, the invention includes hostcells containing a polynucleotide encoding an antibody of the invention,or a heavy or light chain thereof, or a single chain antibody, operablylinked to a heterologous promoter. In preferred embodiments for theexpression of double-chained antibodies, vectors encoding both the heavyand light chains may be co-expressed in the host cell for expression ofthe entire immunoglobulin molecule, as detailed below.

A variety of host-expression vector systems may be utilized to expressthe antibody molecules of the invention. Such host-expression systemsrepresent vehicles by which the coding sequences of interest may beproduced and subsequently purified, but also represent cells which may,when transformed or transfected with the appropriate nucleotide codingsequences, express an antibody molecule of the invention in situ. Theseinclude but are not limited to microorganisms such as bacteria (e.g., E.coli, B. subtilis) transformed with recombinant bacteriophage DNA,plasmid DNA or cosmid DNA expression vectors containing antibody codingsequences; yeast (e.g., Saccharomyces, Pichia) transformed withrecombinant yeast expression vectors containing antibody codingsequences; insect cell systems infected with recombinant virusexpression vectors (e.g., baculovirus) containing antibody codingsequences; plant cell systems infected with recombinant virus expressionvectors (e.g., cauliflower mosaic virus, CaMV; tobacco mosaic virus,TMV) or transformed with recombinant plasmid expression vectors (e.g.,Ti plasmid) containing antibody coding sequences; or mammalian cellsystems (e.g., COS, CHO, BHK, 293, 3T3 cells) harboring recombinantexpression constructs containing promoters derived from the genome ofmammalian cells (e.g., metallothionein promoter) or from mammalianviruses (e.g., the adenovirus late promoter; the vaccinia virus 7.5Kpromoter). Preferably, bacterial cells such as Escherichia coli, andmore preferably, eukaryotic cells, especially for the expression ofwhole recombinant antibody molecule, are used for the expression of arecombinant antibody molecule. For example, mammalian cells such asChinese hamster ovary cells (CHO), in conjunction with a vector such asthe major intermediate early gene promoter element from humancytomegalovirus is an effective expression system for antibodies(Foecking et al., Gene 45:101 (1986); Cockett et al., Bio/Technology 8:2(1990)).

In bacterial systems, a number of expression vectors may beadvantageously selected depending upon the use intended for the antibodymolecule being expressed. For example, when a large quantity of such aprotein is to be produced, for the generation of pharmaceuticalcompositions of an antibody molecule, vectors which direct theexpression of high levels of fusion protein products that are readilypurified may be desirable. Such vectors include, but are not limited, tothe E. coli expression vector pUR278 (Ruther et al., EMBO J. 2:1791(1983)), in which the antibody coding sequence may be ligatedindividually into the vector in frame with the lac Z coding region sothat a fusion protein is produced; pIN vectors (Inouye & Inouye, NucleicAcids Res. 13:3101-3109 (1985); Van Heeke & Schuster, J. Biol. Chem.24:5503-5509 (1989)); and the like. pGEX vectors may also be used toexpress foreign polypeptides as fusion proteins with glutathioneS-transferase (GST). In general, such fusion proteins are soluble andcan easily be purified from lysed cells by adsorption and binding tomatrix glutathione-agarose beads followed by elution in the presence offree glutathione. The pGEX vectors are designed to include thrombin orfactor Xa protease cleavage sites so that the cloned target gene productcan be released from the GST moiety.

In an insect system, Autographa californica nuclear polyhedrosis virus(AcNPV) is used as a vector to express foreign genes. The virus grows inSpodoptera frugiperda cells. The antibody coding sequence may be clonedindividually into non-essential regions (for example the polyhedringene) of the virus and placed under control of an AcNPV promoter (forexample the polyhedrin promoter).

In mammalian host cells, a number of viral-based expression systems maybe utilized. In cases where an adenovirus is used as an expressionvector, the antibody coding sequence of interest may be ligated to anadenovirus transcription/translation control complex, e.g., the latepromoter and tripartite leader sequence. This chimeric gene may then beinserted in the adenovirus genome by in vitro or in vivo recombination.Insertion in a non-essential region of the viral genome (e.g., region E1or E3) will result in a recombinant virus that is viable and capable ofexpressing the antibody molecule in infected hosts. (e.g., see Logan &Shenk, Proc. Natl. Acad. Sci. USA 81:355-359 (1984)). Specificinitiation signals may also be required for efficient translation ofinserted antibody coding sequences. These signals include the ATGinitiation codon and adjacent sequences. Furthermore, the initiationcodon must be in phase with the reading frame of the desired codingsequence to ensure translation of the entire insert. These exogenoustranslational control signals and initiation codons can be of a varietyof origins, both natural and synthetic. The efficiency of expression maybe enhanced by the inclusion of appropriate transcription enhancerelements, transcription terminators, etc. (see Bittner et al., Methodsin Enzymol. 153:51-544 (1987)).

In addition, a host cell strain may be chosen which modulates theexpression of the inserted sequences, or modifies and processes the geneproduct in the specific fashion desired. Such modifications (e.g.,glycosylation) and processing (e.g., cleavage) of protein products maybe important for the function of the protein. Different host cells havecharacteristic and specific mechanisms for the post-translationalprocessing and modification of proteins and gene products. Appropriatecell lines or host systems can be chosen to ensure the correctmodification and processing of the foreign protein expressed. To thisend, eukaryotic host cells which possess the cellular machinery forproper processing of the primary transcript, glycosylation, andphosphorylation of the gene product may be used. Such mammalian hostcells include but are not limited to CHO, VERY, BHK, Hela, COS, MDCK,293, 3T3, WI38, and in particular, breast cancer cell lines such as, forexample, BT483, Hs578T, HTB2, BT20 and T47D, and normal mammary glandcell line such as, for example, CRL7030 and Hs578Bst.

For long-term, high-yield production of recombinant proteins, stableexpression is preferred. For example, cell lines which stably expressthe antibody molecule may be engineered. Rather than using expressionvectors which contain viral origins of replication, host cells can betransformed with DNA controlled by appropriate expression controlelements (e.g., promoter, enhancer, sequences, transcriptionterminators, polyadenylation sites, etc.), and a selectable marker.Following the introduction of the foreign DNA, engineered cells may beallowed to grow for 1-2 days in an enriched media, and then are switchedto a selective media. The selectable marker in the recombinant plasmidconfers resistance to the selection and allows cells to stably integratethe plasmid into their chromosomes and grow to form foci which in turncan be cloned and expanded into cell lines. This method mayadvantageously be used to engineer cell lines which express the antibodymolecule. Such engineered cell lines may be particularly useful inscreening and evaluation of compounds that interact directly orindirectly with the antibody molecule.

A number of selection systems may be used, including but not limited tothe herpes simplex virus thymidine kinase (Wigler et al., Cell 11:223(1977)), hypoxanthine-guanine phosphoribosyltransferase (Szybalska &Szybalski, Proc. Natl. Acad. Sci. USA 48:202 (1992)), and adeninephosphoribosyltransferase (Lowy et al., Cell 22:817 (1980)) genes can beemployed in tk−, hgprt− or aprt− cells, respectively. Also,antimetabolite resistance can be used as the basis of selection for thefollowing genes: dhfr, which confers resistance to methotrexate (Wigleret al., Natl. Acad. Sci. USA 77:357 (1980); O'Hare et al., Proc. Natl.Acad. Sci. USA 78:1527 (1981)); gpt, which confers resistance tomycophenolic acid (Mulligan & Berg, Proc. Natl. Acad. Sci. USA 78:2072(1981)); neo, which confers resistance to the aminoglycoside G-418Clinical Pharmacy 12:488-505; Wu and Wu, Biotherapy 3:87-95 (1991);Tolstoshev, Ann. Rev. Pharmacol. Toxicol. 32:573-596 (1993); Mulligan,Science 260:926-932 (1993); and Morgan and Anderson, Ann. Rev. Biochem.62:191-217 (1993); May, 1993, TIB TECH 11(5):155-215 (1993)); and hygro,which confers resistance to hygromycin (Santerre et al., Gene 30:147(1984)). Methods commonly known in the art of recombinant DNA technologymay be routinely applied to select the desired recombinant clone, andsuch methods are described, for example, in Ausubel et al. (eds.),Current Protocols in Molecular Biology, John Wiley & Sons, NY (1993);Kriegler, Gene Transfer and Expression, A Laboratory Manual, StocktonPress, NY (1990); and in Chapters 12 and 13, Dracopoli et al. (eds),Current Protocols in Human Genetics, John Wiley & Sons, NY (1994);Colberre-Garapin et al., J. Mol. Biol. 150:1 (1981), which areincorporated by reference herein in their entireties.

The expression levels of an antibody molecule can be increased by vectoramplification (for a review, see Bebbington and Hentschel, The use ofvectors based on gene amplification for the expression of cloned genesin mammalian cells in DNA cloning, Vol. 3. (Academic Press, New York,1987)). When a marker in the vector system expressing antibody isamplifiable, increase in the level of inhibitor present in culture ofhost cell will increase the number of copies of the marker gene. Sincethe amplified region is associated with the antibody gene, production ofthe antibody will also increase (Crouse et al., Mol. Cell. Biol. 3:257(1983)).

Vectors which use glutamine synthase (GS) or DHFR as the selectablemarkers can be amplified in the presence of the drugs methioninesulphoximine or methotrexate, respectively. An advantage of glutaminesynthase based vectors are the availability of cell lines (e.g., themurine myeloma cell line, NS0) which are glutamine synthase negative.Glutamine synthase expression systems can also function in glutaminesynthase expressing cells (e.g. Chinese Hamster Ovary (CHO) cells) byproviding additional inhibitor to prevent the functioning of theendogenous gene. A glutamine synthase expression system and componentsthereof are detailed in PCT publications: WO87/04462; WO86/05807;WO89/01036; WO89/10404; and WO91/06657 which are incorporated in theirentireties by reference herein. Additionally, glutamine synthaseexpression vectors that may be used according to the present inventionare commercially available from suppliers, including, for example LonzaBiologics, Inc. (Portsmouth, N.H.). Expression and production ofmonoclonal antibodies using a GS expression system in murine myelomacells is described in Bebbington et al., Bio/technology 10:169(1992) andin Biblia and Robinson Biotechnol. Prog. 11:1 (1995) which areincorporated in their entireties by reference herein.

The host cell may be co-transfected with two expression vectors of theinvention, the first vector encoding a heavy chain derived polypeptideand the second vector encoding a light chain derived polypeptide. Thetwo vectors may contain identical selectable markers which enable equalexpression of heavy and light chain polypeptides. Alternatively, asingle vector may be used which encodes, and is capable of expressing,both heavy and light chain polypeptides. In such situations, the lightchain should be placed before the heavy chain to avoid an excess oftoxic free heavy chain (Proudfoot, Nature 322:52 (1986); Kohler, Proc.Natl. Acad. Sci. USA 77:2197 (1980)). The coding sequences for the heavyand light chains may comprise cDNA or genomic DNA.

Once an antibody molecule of the invention has been produced by ananimal, chemically synthesized, or recombinantly expressed, it may bepurified by any method known in the art for purification of animmunoglobulin molecule, for example, by chromatography (e.g., ionexchange, affinity, particularly by affinity for the specific antigenafter Protein A, and sizing column chromatography), centrifugation,differential solubility, or by any other standard technique for thepurification of proteins. In addition, the antibodies that bind to aTherapeutic protein and that may correspond to a Therapeutic proteinportion of an albumin fusion protein of the invention or fragmentsthereof can be fused to heterologous polypeptide sequences describedherein or otherwise known in the art, to facilitate purification.

Modifications of Antibodies

Antibodies that bind a Therapeutic protein or fragments or variants canbe fused to marker sequences, such as a peptide to facilitatepurification. In preferred embodiments, the marker amino acid sequenceis a hexa-histidine peptide, such as the tag provided in a pQE vector(QIAGEN, Inc., 9259 Eton Avenue, Chatsworth, Calif., 91311), amongothers, many of which are commercially available. As described in Gentzet al., Proc. Natl. Acad. Sci. USA 86:821-824 (1989), for instance,hexa-histidine provides for convenient purification of the fusionprotein. Other peptide tags useful for purification include, but are notlimited to, the hemagglutinin tag (also called the “HA tag”), whichcorresponds to an epitope derived from the influenza hemagglutininprotein (Wilson et al., Cell 37:767 (1984)) and the “flag” tag.

The present invention further encompasses antibodies or fragmentsthereof conjugated to a diagnostic or therapeutic agent. The antibodiescan be used diagnostically to, for example, monitor the development orprogression of a tumor as part of a clinical testing procedure to, e.g.,determine the efficacy of a given treatment regimen. Detection can befacilitated by coupling the antibody to a detectable substance. Examplesof detectable substances include various enzymes, prosthetic groups,fluorescent materials, luminescent materials, bioluminescent materials,radioactive materials, positron emitting metals using various positronemission tomographies, and nonradioactive paramagnetic metal ions. Thedetectable substance may be coupled or conjugated either directly to theantibody (or fragment thereof) or indirectly, through an intermediate(such as, for example, a linker known in the art) using techniques knownin the art. See, for example, U.S. Pat. No. 4,741,900 for metal ionswhich can be conjugated to antibodies for use as diagnostics accordingto the present invention. Examples of suitable enzymes includehorseradish peroxidase, alkaline phosphatase, beta-galactosidase, oracetylcholinesterase; examples of suitable prosthetic group complexesinclude streptavidin/biotin and avidin/biotin; examples of suitablefluorescent materials include umbelliferone, fluorescein, fluoresceinisothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansylchloride or phycoerythrin; an example of a luminescent material includesluminol; examples of bioluminescent materials include luciferase,luciferin, and aequorin; and examples of suitable radioactive materialinclude 125I, 131I, 111In or 99Tc. Other examples of detectablesubstances have been described elsewhere herein.

Further, an antibody of the invention may be conjugated to a therapeuticmoiety such as a cytotoxin, e.g., a cytostatic or cytocidal agent, atherapeutic agent or a radioactive metal ion, e.g., alpha-emitters suchas, for example, 213Bi. A cytotoxin or cytotoxic agent includes anyagent that is detrimental to cells. Examples include paclitaxol,cytochalasin B, gramicidin D, ethidium bromide, emetine, mitomycin,etoposide, tenoposide, vincristine, vinblastine, colchicin, doxorubicin,daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin,actinomycin D, 1-dehydrotestosterone, glucocorticoids, procaine,tetracaine, lidocaine, propranolol, and puromycin and analogs orhomologs thereof. Therapeutic agents include, but are not limited to,antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine,cytarabine, 5-fluorouracil decarbazine), alkylating agents (e.g.,mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BSNU) andlomustine (CCNU), cyclothosphamide, busulfan, dibromomannitol,streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP)cisplatin), anthracyclines (e.g., daunorubicin (formerly daunomycin) anddoxorubicin), antibiotics (e.g., dactinomycin (formerly actinomycin),bleomycin, mithramycin, and anthramycin (AMC)), and anti-mitotic agents(e.g., vincristine and vinblastine).

The conjugates of the invention can be used for modifying a givenbiological response, the therapeutic agent or drug moiety is not to beconstrued as limited to classical chemical therapeutic agents. Forexample, the drug moiety may be a protein or polypeptide possessing adesired biological activity. Such proteins may include, for example, atoxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin;a protein such as tumor necrosis factor, alpha-interferon, β-interferon,nerve growth factor, platelet derived growth factor, tissue plasminogenactivator, an apoptotic agent, e.g., TNF-alpha, TNF-beta, AIM I (See,International Publication No. WO 97/33899), AIM II (See, InternationalPublication No. WO 97/34911), Fas Ligand (Takahashi et al., Int.Immunol., 6:1567-1574 (1994)), VEGI (See, International Publication No.WO 99/23105), a thrombotic agent or an anti-angiogenic agent, e.g.,angiostatin or endostatin; or, biological response modifiers such as,for example, lymphokines, interleukin-1 (“IL-1”), interleukin-2(“IL-2”), interleukin-6 (“IL-6”), granulocyte macrophage colonystimulating factor (“GM-CSF”), granulocyte colony stimulating factor(“G-CSF”), or other growth factors.

Antibodies may also be attached to solid supports, which areparticularly useful for immunoassays or purification of the targetantigen. Such solid supports include, but are not limited to, glass,cellulose, polyacrylamide, nylon, polystyrene, polyvinyl chloride orpolypropylene.

Techniques for conjugating such therapeutic moiety to antibodies arewell known. See, for example, Arnon et al., “Monoclonal Antibodies ForImmunotargeting Of Drugs In Cancer Therapy”, in Monoclonal AntibodiesAnd Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56 (Alan R. Liss,Inc. 1985); Hellstrom et al., “Antibodies For Drug Delivery”, inControlled Drug Delivery (2nd Ed.), Robinson et al. (eds.), pp. 623-53(Marcel Dekker, Inc. 1987); Thorpe, “Antibody Carriers Of CytotoxicAgents In Cancer Therapy: A Review”, in Monoclonal Antibodies '84:Biological And Clinical Applications, Pinchera et al. (eds.), pp.475-506 (1985); “Analysis, Results, And Future Prospective Of TheTherapeutic Use Of Radiolabeled Antibody In Cancer Therapy”, inMonoclonal Antibodies For Cancer Detection And Therapy, Baldwin et al.(eds.), pp. 303-16 (Academic Press 1985), and Thorpe et al., “ThePreparation And Cytotoxic Properties Of Antibody-Toxin Conjugates”,Immunol. Rev. 62:119-58 (1982).

Alternatively, an antibody can be conjugated to a second antibody toform an antibody heteroconjugate as described by Segal in U.S. Pat. No.4,676,980, which is incorporated herein by reference in its entirety.

An antibody, with or without a therapeutic moiety conjugated to it,administered alone or in combination with cytotoxic factor(s) and/orcytokine(s) can be used as a therapeutic.

Antibody-Albumin Fusion

Antibodies that bind to a Therapeutic protein and that may correspond toa Therapeutic protein portion of an albumin fusion protein of theinvention include, but are not limited to, antibodies that bind aTherapeutic protein disclosed in the “Therapeutic Protein X” column ofTable 1, or a fragment or variant thereof

In specific embodiments, the fragment or variant of an antibody thatimmunospecifcally binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, the VH domain. In other embodiments, thefragment or variant of an antibody that immunospecifcally binds aTherapeutic protein and that corresponds to a Therapeutic proteinportion of an albumin fusion protein comprises, or alternativelyconsists of, one, two or three VH CDRs. In other embodiments, thefragment or variant of an antibody that immunospecifcally binds aTherapeutic protein and that corresponds to a Therapeutic proteinportion of an albumin fusion protein comprises, or alternativelyconsists of, the VH CDR1. In other embodiments, the fragment or variantof an antibody that immunospecifcally binds a Therapeutic protein andthat corresponds to a Therapeutic protein portion of an albumin fusionprotein comprises, or alternatively consists of, the VH CDR2. In otherembodiments, the fragment or variant of an antibody thatimmunospecifcally binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, the VH CDR3.

In specific embodiments, the fragment or variant of an antibody thatimmunospecifcally binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, the VL domain. In other embodiments, thefragment or variant of an antibody that immunospecifcally binds aTherapeutic protein and that corresponds to a Therapeutic proteinportion of an albumin fusion protein comprises, or alternativelyconsists of, one, two or three VL CDRs. In other embodiments, thefragment or variant of an antibody that immunospecifcally binds aTherapeutic protein and that corresponds to a Therapeutic proteinportion of an albumin fusion protein comprises, or alternativelyconsists of, the VL CDR1. In other embodiments, the fragment or variantof an antibody that immunospecifcally binds a Therapeutic protein andthat corresponds to a Therapeutic protein portion of an albumin fusionprotein comprises, or alternatively consists of, the VL CDR2. In otherembodiments, the fragment or variant of an antibody thatimmunospecifcally binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, the VL CDR3.

In other embodiments, the fragment or variant of an antibody thatimmunospecifcally binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, one, two, three, four, five, or six VH and/orVL CDRs.

In preferred embodiments, the fragment or variant of an antibody thatimmunospecifically binds a Therapeutic protein and that corresponds to aTherapeutic protein portion of an albumin fusion protein comprises, oralternatively consists of, an scFv comprising the VH domain of theTherapeutic antibody, linked to the VL domain of the therapeuticantibody by a peptide linker such as (Gly₄Ser)₃ (SEQ ID NO:1092).

Immunophenotyping

The antibodies of the invention or albumin fusion proteins of theinvention comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein (or fragment or variant thereof) may beutilized for immunophenotyping of cell lines and biological samples.Therapeutic proteins of the present invention may be useful ascell-specific markers, or more specifically as cellular markers that aredifferentially expressed at various stages of differentiation and/ormaturation of particular cell types. Monoclonal antibodies (or albuminfusion proteins comprising at least a fragment or variant of an antibodythat binds a Therapeutic protein) directed against a specific epitope,or combination of epitopes, will allow for the screening of cellularpopulations expressing the marker. Various techniques can be utilizedusing monoclonal antibodies (or albumin fusion proteins comprising atleast a fragment or variant of an antibody that binds a Therapeuticprotein) to screen for cellular populations expressing the marker(s),and include magnetic separation using antibody-coated magnetic beads,“panning” with antibody attached to a solid matrix (i.e., plate), andflow cytometry (See, e.g., U.S. Pat. No. 5,985,660; and Morrison et al.,Cell, 96:737-49 (1999)).

These techniques allow for the screening of particular populations ofcells, such as might be found with hematological malignancies (i.e.minimal residual disease (MRD) in acute leukemic patients) and“non-self” cells in transplantations to prevent Graft-versus-HostDisease (GVHD). Alternatively, these techniques allow for the screeningof hematopoietic stem and progenitor cells capable of undergoingproliferation and/or differentiation, as might be found in humanumbilical cord blood.

Characterizing Antibodies that Bind a Therapeutic Protein and AlbuminFusion Proteins Comprising a Fragment or Variant of an Antibody thatBinds a Therapeutic Protein

The antibodies of the invention or albumin fusion proteins of theinvention comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein (or fragment or variant thereof) may becharacterized in a variety of ways. In particular, Albumin fusionproteins of the invention comprising at least a fragment or variant ofan antibody that binds a Therapeutic protein may be assayed for theability to specifically bind to the same antigens specifically bound bythe antibody that binds a Therapeutic protein corresponding to theantibody that binds a Therapeutic protein portion of the albumin fusionprotein using techniques described herein or routinely modifyingtechniques known in the art.

Assays for the ability of the antibodies of the invention or albuminfusion proteins of the invention comprising at least a fragment orvariant of an antibody that binds a Therapeutic protein (or fragment orvariant thereof) to (specifically) bind a specific protein or epitopemay be performed in solution (e.g., Houghten, Bio/Techniques13:412-421(1992)), on beads (e.g., Lam, Nature 354:82-84 (1991)), onchips (e.g., Fodor, Nature 364:555-556 (1993)), on bacteria (e.g., U.S.Pat. No. 5,223,409), on spores (e.g., U.S. Pat. Nos. 5,571,698;5,403,484; and 5,223,409), on plasmids (e.g., Cull et al., Proc. Natl.Acad. Sci. USA 89:1865-1869 (1992)) or on phage (e.g., Scott and Smith,Science 249:386-390 (1990); Devlin, Science 249:404-406 (1990); Cwirlaet al., Proc. Natl. Acad. Sci. USA 87:6378-6382 (1990); and Felici, J.Mol. Biol. 222:301-310 (1991)) (each of these references is incorporatedherein in its entirety by reference). The antibodies of the invention oralbumin fusion proteins of the invention comprising at least a fragmentor variant of an antibody that binds a Therapeutic protein (or fragmentor variant thereof) may also be assayed for their specificity andaffinity for a specific protein or epitope using or routinely modifyingtechniques described herein or otherwise known in the art.

The albumin fusion proteins of the invention comprising at least afragment or variant of an antibody that binds a Therapeutic protein maybe assayed for cross-reactivity with other antigens (e.g., moleculesthat have sequence/structure conservation with the molecule(s)specifically bound by the antibody that binds a Therapeutic protein (orfragment or variant thereof) corresponding to the Therapeutic proteinportion of the albumin fusion protein of the invention) by any methodknown in the art.

Immunoassays which can be used to analyze (immunospecific) binding andcross-reactivity include, but are not limited to, competitive andnon-competitive assay systems using techniques such as western blots,radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich”immunoassays, immunoprecipitation assays, precipitin reactions, geldiffusion precipitin reactions, immunodiffusion assays, agglutinationassays, complement-fixation assays, immunoradiometric assays,fluorescent immunoassays, and protein A immunoassays, to name but a few.Such assays are routine and well known in the art (see, e.g., Ausubel etal, eds, 1994, Current Protocols in Molecular Biology, Vol. 1, JohnWiley & Sons, Inc., New York, which is incorporated by reference hereinin its entirety). Exemplary immunoassays are described briefly below(but are not intended by way of limitation).

Immunoprecipitation protocols generally comprise lysing a population ofcells in a lysis buffer such as RIPA buffer (1% NP-40 or Triton X-100,1% sodium deoxycholate, 0.1% SDS, 0.15 M NaCl, 0.01 M sodium phosphateat pH 7.2, 1% Trasylol) supplemented with protein phosphatase and/orprotease inhibitors (e.g., EDTA, PMSF, aprotinin, sodium vanadate),adding an antibody of the invention or albumin fusion protein of theinvention comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein (or fragment or variant thereof) to the celllysate, incubating for a period of time (e.g., 1 to 4 hours) at 40degrees C., adding protein A and/or protein G sepharose beads (or beadscoated with an appropriate anti-idiotypic antibody or anti-albuminantibody in the case when an albumin fusion protein comprising at leasta fragment or variant of a Therapeutic antibody) to the cell lysate,incubating for about an hour or more at 40 degrees C., washing the beadsin lysis buffer and resuspending the beads in SDS/sample buffer. Theability of the antibody or albumin fusion protein of the invention toimmunoprecipitate a particular antigen can be assessed by, e.g., westernblot analysis. One of skill in the art would be knowledgeable as to theparameters that can be modified to increase the binding of the antibodyor albumin fusion protein to an antigen and decrease the background(e.g., pre-clearing the cell lysate with sepharose beads). For furtherdiscussion regarding immunoprecipitation protocols see, e.g., Ausubel etal, eds, 1994, Current Protocols in Molecular Biology, Vol. 1, JohnWiley & Sons, Inc., New York at 10.16.1.

Western blot analysis generally comprises preparing protein samples,electrophoresis of the protein samples in a polyacrylamide gel (e.g.,8%-20% SDS-PAGE depending on the molecular weight of the antigen),transferring the protein sample from the polyacrylamide gel to amembrane such as nitrocellulose, PVDF or nylon, blocking the membrane inblocking solution (e.g., PBS with 3% BSA or non-fat milk), washing themembrane in washing buffer (e.g., PBS-Tween 20), applying the antibodyor albumin fusion protein of the invention (diluted in blocking buffer)to the membrane, washing the membrane in washing buffer, applying asecondary antibody (which recognizes the albumin fusion protein, e.g.,an anti-human serum albumin antibody) conjugated to an enzymaticsubstrate (e.g., horseradish peroxidase or alkaline phosphatase) orradioactive molecule (e.g., ³²P or ¹²⁵I) diluted in blocking buffer,washing the membrane in wash buffer, and detecting the presence of theantigen. One of skill in the art would be knowledgeable as to theparameters that can be modified to increase the signal detected and toreduce the background noise. For further discussion regarding westernblot protocols see, e.g., Ausubel et al, eds, 1994, Current Protocols inMolecular Biology, Vol. 1, John Wiley & Sons, Inc., New York at 10.8.1.

ELISAs comprise preparing antigen, coating the well of a 96-wellmicrotiter plate with the antigen, washing away antigen that did notbind the wells, adding the antibody or albumin fusion protein(comprising at least a fragment or variant of an antibody that binds aTherapeutic protein) of the invention conjugated to a detectablecompound such as an enzymatic substrate (e.g., horseradish peroxidase oralkaline phosphatase) to the wells and incubating for a period of time,washing away unbound or non-specifically bound albumin fusion proteins,and detecting the presence of the antibody or albumin fusion proteinsspecifically bound to the antigen coating the well. In ELISAs theantibody or albumin fusion protein does not have to be conjugated to adetectable compound; instead, a second antibody (which recognizes theantibody or albumin fusion protein, respectively) conjugated to adetectable compound may be added to the well. Further, instead ofcoating the well with the antigen, antibody or the albumin fusionprotein may be coated to the well. In this case, the detectable moleculecould be the antigen conjugated to a detectable compound such as anenzymatic substrate (e.g., horseradish peroxidase or alkalinephosphatase). One of skill in the art would be knowledgeable as to theparameters that can be modified to increase the signal detected as wellas other variations of ELISAs known in the art. For further discussionregarding ELISAs see, e.g., Ausubel et al, eds, 1994, Current Protocolsin Molecular Biology, Vol. 1, John Wiley & Sons, Inc., New York at11.2.1.

The binding affinity of an albumin fusion protein to a protein, antigen,or epitope and the off-rate of an antibody- or albumin fusionprotein-protein/antigen/epitope interaction can be determined bycompetitive binding assays. One example of a competitive binding assayis a radioimmunoassay comprising the incubation of labeled antigen(e.g., ³H or ¹²⁵I) with the antibody or albumin fusion protein of theinvention in the presence of increasing amounts of unlabeled antigen,and the detection of the antibody bound to the labeled antigen. Theaffinity of the antibody or albumin fusion protein of the invention fora specific protein, antigen, or epitope and the binding off-rates can bedetermined from the data by Scatchard plot analysis. Competition with asecond protein that binds the same protein, antigen or epitope as theantibody or albumin fusion protein, can also be determined usingradioimmunoassays. In this case, the protein, antigen or epitope isincubated with an antibody or albumin fusion protein of the inventionconjugated to a labeled compound (e.g., ³H or ¹²⁵I) in the presence ofincreasing amounts of an unlabeled second protein that binds the sameprotein, antigen, or epitope as the albumin fusion protein of theinvention.

In a preferred embodiment, BIAcore kinetic analysis is used to determinethe binding on and off rates of antibody or albumin fusion proteins ofthe invention to a protein, antigen or epitope. BIAcore kinetic analysiscomprises analyzing the binding and dissociation of antibodies, albuminfusion proteins, or specific polypeptides, antigens or epitopes fromchips with immobilized specific polypeptides, antigens or epitopes,antibodies or albumin fusion proteins, respectively, on their surface.

Therapeutic Uses

The present invention is further directed to antibody-based therapieswhich involve administering antibodies of the invention or albuminfusion proteins of the invention comprising at least a fragment orvariant of an antibody that binds a Therapeutic protein to an animal,preferably a mammal, and most preferably a human, patient for treatingone or more of the disclosed diseases, disorders, or conditions.Therapeutic compounds of the invention include, but are not limited to,antibodies of the invention (including fragments, analogs andderivatives thereof as described herein), nucleic acids encodingantibodies of the invention (including fragments, analogs andderivatives thereof and anti-idiotypic antibodies as described herein),albumin fusion proteins of the invention comprising at least a fragmentor variant of an antibody that binds a Therapeutic protein, and nucleicacids encoding such albumin fusion proteins. The antibodies of theinvention or albumin fusion proteins of the invention comprising atleast a fragment or variant of an antibody that binds a Therapeuticprotein can be used to treat, inhibit or prevent diseases, disorders orconditions associated with aberrant expression and/or activity of aTherapeutic protein, including, but not limited to, any one or more ofthe diseases, disorders, or conditions described herein. The treatmentand/or prevention of diseases, disorders, or conditions associated withaberrant expression and/or activity of a Therapeutic protein includes,but is not limited to, alleviating symptoms associated with thosediseases, disorders or conditions. antibodies of the invention oralbumin fusion proteins of the invention comprising at least a fragmentor variant of an antibody that binds a Therapeutic protein may beprovided in pharmaceutically acceptable compositions as known in the artor as described herein.

In a specific and preferred embodiment, the present invention isdirected to antibody-based therapies which involve administeringantibodies of the invention or albumin fusion proteins of the inventioncomprising at least a fragment or variant of an antibody that binds aTherapeutic protein to an animal, preferably a mammal, and mostpreferably a human, patient for treating one or more diseases,disorders, or conditions, including but not limited to: neuraldisorders, immune system disorders, muscular disorders, reproductivedisorders, gastrointestinal disorders, pulmonary disorders,cardiovascular disorders, renal disorders, proliferative disorders,and/or cancerous diseases and conditions., and/or as described elsewhereherein. Therapeutic compounds of the invention include, but are notlimited to, antibodies of the invention (e.g., antibodies directed tothe full length protein expressed on the cell surface of a mammaliancell; antibodies directed to an epitope of a Therapeutic protein andnucleic acids encoding antibodies of the invention (including fragments,analogs and derivatives thereof and anti-idiotypic antibodies asdescribed herein). The antibodies of the invention can be used to treat,inhibit or prevent diseases, disorders or conditions associated withaberrant expression and/or activity of a Therapeutic protein, including,but not limited to, any one or more of the diseases, disorders, orconditions described herein. The treatment and/or prevention ofdiseases, disorders, or conditions associated with aberrant expressionand/or activity of a Therapeutic protein includes, but is not limitedto, alleviating symptoms associated with those diseases, disorders orconditions. Antibodies of the invention or albumin fusion proteins ofthe invention comprising at least a fragment or variant of an antibodythat binds a Therapeutic protein may be provided in pharmaceuticallyacceptable compositions as known in the art or as described herein.

A summary of the ways in which the antibodies of the invention oralbumin fusion proteins of the invention comprising at least a fragmentor variant of an antibody that binds a Therapeutic protein may be usedtherapeutically includes binding Therapeutic proteins locally orsystemically in the body or by direct cytotoxicity of the antibody, e.g.as mediated by complement (CDC) or by effector cells (ADCC). Some ofthese approaches are described in more detail below. Armed with theteachings provided herein, one of ordinary skill in the art will knowhow to use the antibodies of the invention or albumin fusion proteins ofthe invention comprising at least a fragment or variant of an antibodythat binds a Therapeutic protein for diagnostic, monitoring ortherapeutic purposes without undue experimentation.

The antibodies of the invention or albumin fusion proteins of theinvention comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein may be advantageously utilized incombination with other monoclonal or chimeric antibodies, or withlymphokines or hematopoietic growth factors (such as, e.g., IL-2, IL-3and IL-7), for example, which serve to increase the number or activityof effector cells which interact with the antibodies.

The antibodies of the invention or albumin fusion proteins of theinvention comprising at least a fragment or variant of an antibody thatbinds a Therapeutic protein may be administered alone or in combinationwith other types of treatments (e.g., radiation therapy, chemotherapy,hormonal therapy, immunotherapy and anti-tumor agents). Generally,administration of products of a species origin or species reactivity (inthe case of antibodies) that is the same species as that of the patientis preferred. Thus, in a preferred embodiment, human antibodies,fragments derivatives, analogs, or nucleic acids, are administered to ahuman patient for therapy or prophylaxis.

It is preferred to use high affinity and/or potent in vivo inhibitingand/or neutralizing antibodies against Therapeutic proteins, fragmentsor regions thereof, (or the albumin fusion protein correlate of such anantibody) for both immunoassays directed to and therapy of disordersrelated to polynucleotides or polypeptides, including fragments thereof,of the present invention. Such antibodies, fragments, or regions, willpreferably have an affinity for polynucleotides or polypeptides of theinvention, including fragments thereof. Preferred binding affinitiesinclude dissociation constants or Kd's less than 5×10⁻² M, 10⁻² M,5×10⁻³ M, 10⁻³ M, 5×10⁻⁴ M, 10⁻⁴ M. More preferred binding affinitiesinclude those with a dissociation constant or Kd less than 5×10⁻⁵ M,10⁻⁵ M, 5×10⁻⁶ M, 10⁻⁶M, 5×10⁻⁷ M, 10⁷ M, 5×10⁻⁸ M or 10⁻⁸ M. Even morepreferred binding affinities include those with a dissociation constantor Kd less than 5×10⁻⁹ M, 10⁻⁹ M, 5×10⁻¹⁰ M, 10⁻¹⁰ M, 5×10⁻¹¹ M, 10⁻¹¹M, 5×10⁻¹² M, 10⁻¹² M, 5×10⁻¹³ M, 10⁻¹³ M, 5×10⁻¹⁴ M, 10⁻¹⁴ M, 5×10⁻¹⁵M, or 10⁻¹⁵ M.

Gene Therapy

In a specific embodiment, nucleic acids comprising sequences encodingantibodies that bind therapeutic proteins or albumin fusion proteinscomprising at least a fragment or variant of an antibody that binds aTherapeutic protein are administered to treat, inhibit or prevent adisease or disorder associated with aberrant expression and/or activityof a Therapeutic protein, by way of gene therapy. Gene therapy refers totherapy performed by the administration to a subject of an expressed orexpressible nucleic acid. In this embodiment of the invention, thenucleic acids produce their encoded protein that mediates a therapeuticeffect.

Any of the methods for gene therapy available in the art can be usedaccording to the present invention. Exemplary methods are described inmore detail elsewhere in this application.

Demonstration of Therapeutic or Prophylactic Activity

The compounds or pharmaceutical compositions of the invention arepreferably tested in vitro, and then in vivo for the desired therapeuticor prophylactic activity, prior to use in humans. For example, in vitroassays to demonstrate the therapeutic or prophylactic utility of acompound or pharmaceutical composition include, the effect of a compoundon a cell line or a patient tissue sample. The effect of the compound orcomposition on the cell line and/or tissue sample can be determinedutilizing techniques known to those of skill in the art including, butnot limited to, rosette formation assays and cell lysis assays. Inaccordance with the invention, in vitro assays which can be used todetermine whether administration of a specific compound is indicated,include in vitro cell culture assays in which a patient tissue sample isgrown in culture, and exposed to or otherwise administered a compound,and the effect of such compound upon the tissue sample is observed.

Therapeutic/Prophylactic Administration and Composition

The invention provides methods of treatment, inhibition and prophylaxisby administration to a subject of an effective amount of a compound orpharmaceutical composition of the invention. In a preferred embodiment,the compound is substantially purified (e.g., substantially free fromsubstances that limit its effect or produce undesired side-effects). Thesubject is preferably an animal, including but not limited to animalssuch as cows, pigs, horses, chickens, cats, dogs, etc., and ispreferably a mammal, and most preferably human.

Formulations and methods of administration that can be employed when thecompound comprises a nucleic acid or an immunoglobulin are describedabove; additional appropriate formulations and routes of administrationcan be selected from among those described herein below.

Various delivery systems are known and can be used to administer acompound of the invention, e.g., encapsulation in liposomes,microparticles, microcapsules, recombinant cells capable of expressingthe compound, receptor-mediated endocytosis (see, e.g., Wu and Wu, J.Biol. Chem. 262:4429-4432 (1987)), construction of a nucleic acid aspart of a retroviral or other vector, etc. Methods of introductioninclude but are not limited to intradermal, intramuscular,intraperitoneal, intravenous, subcutaneous, intranasal, epidural, andoral routes. The compounds or compositions may be administered by anyconvenient route, for example by infusion or bolus injection, byabsorption through epithelial or mucocutaneous linings (e.g., oralmucosa, rectal and intestinal mucosa, etc.) and may be administeredtogether with other biologically active agents. Administration can besystemic or local. In addition, it may be desirable to introduce thepharmaceutical compounds or compositions of the invention into thecentral nervous system by any suitable route, including intraventricularand intrathecal injection; intraventricular injection may be facilitatedby an intraventricular catheter, for example, attached to a reservoir,such as an Ommaya reservoir. Pulmonary administration can also beemployed, e.g., by use of an inhaler or nebulizer, and formulation withan aerosolizing agent.

In a specific embodiment, it may be desirable to administer thepharmaceutical compounds or compositions of the invention locally to thearea in need of treatment; this may be achieved by, for example, and notby way of limitation, local infusion during surgery, topicalapplication, e.g., in conjunction with a wound dressing after surgery,by injection, by means of a catheter, by means of a suppository, or bymeans of an implant, said implant being of a porous, non-porous, orgelatinous material, including membranes, such as sialastic membranes,or fibers. Preferably, when administering a protein, including anantibody, of the invention, care must be taken to use materials to whichthe protein does not absorb.

In another embodiment, the compound or composition can be delivered in avesicle, in particular a liposome (see Langer, Science 249:1527-1533(1990); Treat et al., in Liposomes in the Therapy of Infectious Diseaseand Cancer, Lopez-Berestein and Fidler (eds.), Liss, New York, pp.353-365 (1989); Lopez-Berestein, ibid., pp. 317-327; see generallyibid.)

In yet another embodiment, the compound or composition can be deliveredin a controlled release system. In one embodiment, a pump may be used(see Langer, supra; Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987);Buchwald et al., Surgery 88:507 (1980); Saudek et al., N. Engl. J. Med.321:574 (1989)). In another embodiment, polymeric materials can be used(see Medical Applications of Controlled Release, Langer and Wise (eds.),CRC Pres., Boca Raton, Fla. (1974); Controlled Drug Bioavailability,Drug Product Design and Performance, Smolen and Ball (eds.), Wiley, NewYork (1984); Ranger and Peppas, J., Macromol. Sci. Rev. Macromol. Chem.23:61 (1983); see also Levy et al., Science 228:190 (1985); During etal., Ann. Neurol. 25:351 (1989); Howard et al., J. Neurosurg. 71:105(1989)). In yet another embodiment, a controlled release system can beplaced in proximity of the therapeutic target, e.g., the brain, thusrequiring only a fraction of the systemic dose (see, e.g., Goodson, inMedical Applications of Controlled Release, supra, vol. 2, pp. 115-138(1984)).

Other controlled release systems are discussed in the review by Langer(Science 249:1527-1533 (1990)).

In a specific embodiment where the compound of the invention is anucleic acid encoding a protein, the nucleic acid can be administered invivo to promote expression of its encoded protein, by constructing it aspart of an appropriate nucleic acid expression vector and administeringit so that it becomes intracellular, e.g., by use of a retroviral vector(see U.S. Pat. No. 4,980,286), or by direct injection, or by use ofmicroparticle bombardment (e.g., a gene gun; Biolistic, Dupont), orcoating with lipids or cell-surface receptors or transfecting agents, orby administering it in linkage to a homeobox-like peptide which is knownto enter the nucleus (see e.g., Joliot et al., Proc. Natl. Acad. Sci.USA 88:1864-1868 (1991)), etc. Alternatively, a nucleic acid can beintroduced intracellularly and incorporated within host cell DNA forexpression, by homologous recombination.

The present invention also provides pharmaceutical compositions. Suchcompositions comprise a therapeutically effective amount of a compound,and a pharmaceutically acceptable carrier. In a specific embodiment, theterm “pharmaceutically acceptable” means approved by a regulatory agencyof the Federal or a state government or listed in the U.S. Pharmacopeiaor other generally recognized pharmacopeia for use in animals, and moreparticularly in humans. The term “carrier” refers to a diluent,adjuvant, excipient, or vehicle with which the therapeutic isadministered. Such pharmaceutical carriers can be sterile liquids, suchas water and oils, including those of petroleum, animal, vegetable orsynthetic origin, such as peanut oil, soybean oil, mineral oil, sesameoil and the like. Water is a preferred carrier when the pharmaceuticalcomposition is administered intravenously. Saline solutions and aqueousdextrose and glycerol solutions can also be employed as liquid carriers,particularly for injectable solutions. Suitable pharmaceuticalexcipients include starch, glucose, lactose, sucrose, gelatin, malt,rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate,talc, sodium chloride, dried skim milk, glycerol, propylene, glycol,water, ethanol and the like. The composition, if desired, can alsocontain minor amounts of wetting or emulsifying agents, or pH bufferingagents. These compositions can take the form of solutions, suspensions,emulsion, tablets, pills, capsules, powders, sustained-releaseformulations and the like. The composition can be formulated as asuppository, with traditional binders and carriers such astriglycerides. Oral formulation can include standard carriers such aspharmaceutical grades of mannitol, lactose, starch, magnesium stearate,sodium saccharine, cellulose, magnesium carbonate, etc. Examples ofsuitable pharmaceutical carriers are described in “Remington'sPharmaceutical Sciences” by E. W. Martin. Such compositions will containa therapeutically effective amount of the compound, preferably inpurified form, together with a suitable amount of carrier so as toprovide the form for proper administration to the patient. Theformulation should suit the mode of administration.

In a preferred embodiment, the composition is formulated in accordancewith routine procedures as a pharmaceutical composition adapted forintravenous administration to human beings. Typically, compositions forintravenous administration are solutions in sterile isotonic aqueousbuffer. Where necessary, the composition may also include a solubilizingagent and a local anesthetic such as lignocaine to ease pain at the siteof the injection. Generally, the ingredients are supplied eitherseparately or mixed together in unit dosage form, for example, as a drylyophilized powder or water free concentrate in a hermetically sealedcontainer such as an ampoule or sachette indicating the quantity ofactive agent. Where the composition is to be administered by infusion,it can be dispensed with an infusion bottle containing sterilepharmaceutical grade water or saline. Where the composition isadministered by injection, an ampoule of sterile water for injection orsaline can be provided so that the ingredients may be mixed prior toadministration.

The compounds of the invention can be formulated as neutral or saltforms. Pharmaceutically acceptable salts include those formed withanions such as those derived from hydrochloric, phosphoric, acetic,oxalic, tartaric acids, etc., and those formed with cations such asthose derived from sodium, potassium, ammonium, calcium, ferrichydroxides, isopropylamine, triethylamine, 2-ethylamino ethanol,histidine, procaine, etc.

The amount of the compound of the invention which will be effective inthe treatment, inhibition and prevention of a disease or disorderassociated with aberrant expression and/or activity of a Therapeuticprotein can be determined by standard clinical techniques. In addition,in vitro assays may optionally be employed to help identify optimaldosage ranges. The precise dose to be employed in the formulation willalso depend on the route of administration, and the seriousness of thedisease or disorder, and should be decided according to the judgment ofthe practitioner and each patient's circumstances. Effective doses maybe extrapolated from dose-response curves derived from in vitro oranimal model test systems.

For antibodies, the dosage administered to a patient is typically 0.1mg/kg to 100 mg/kg of the patient's body weight. Preferably, the dosageadministered to a patient is between 0.1 mg/kg and 20 mg/kg of thepatient's body weight, more preferably 1 mg/kg to 10 mg/kg of thepatient's body weight. Generally, human antibodies have a longerhalf-life within the human body than antibodies from other species dueto the immune response to the foreign polypeptides. Thus, lower dosagesof human antibodies and less frequent administration is often possible.Further, the dosage and frequency of administration of antibodies of theinvention may be reduced by enhancing uptake and tissue penetration(e.g., into the brain) of the antibodies by modifications such as, forexample, lipidation.

Diagnosis and Imaging

Labeled antibodies and derivatives and analogs thereof that bind aTherapeutic protein (or fragment or variant thereof) (including albuminfusion proteins comprising at least a fragment or variant of an antibodythat binds a Therapeutic protein), can be used for diagnostic purposesto detect, diagnose, or monitor diseases, disorders, and/or conditionsassociated with the aberrant expression and/or activity of Therapeuticprotein. The invention provides for the detection of aberrant expressionof a Therapeutic protein, comprising (a) assaying the expression of theTherapeutic protein in cells or body fluid of an individual using one ormore antibodies specific to the polypeptide interest and (b) comparingthe level of gene expression with a standard gene expression level,whereby an increase or decrease in the assayed Therapeutic proteinexpression level compared to the standard expression level is indicativeof aberrant expression.

The invention provides a diagnostic assay for diagnosing a disorder,comprising (a) assaying the expression of the Therapeutic protein incells or body fluid of an individual using one or more antibodiesspecific to the Therapeutic protein or albumin fusion proteinscomprising at least a fragment of variant of an antibody specific to aTherapeutic protein, and (b) comparing the level of gene expression witha standard gene expression level, whereby an increase or decrease in theassayed Therapeutic protein gene expression level compared to thestandard expression level is indicative of a particular disorder. Withrespect to cancer, the presence of a relatively high amount oftranscript in biopsied tissue from an individual may indicate apredisposition for the development of the disease, or may provide ameans for detecting the disease prior to the appearance of actualclinical symptoms. A more definitive diagnosis of this type may allowhealth professionals to employ preventative measures or aggressivetreatment earlier thereby preventing the development or furtherprogression of the cancer.

Antibodies of the invention or albumin fusion proteins comprising atleast a fragment of variant of an antibody specific to a Therapeuticprotein can be used to assay protein levels in a biological sample usingclassical immunohistological methods known to those of skill in the art(e.g., see Jalkanen et al., J. Cell. Biol. 101:976-985 (1985); Jalkanenet al., J. Cell. Biol. 105:3087-3096 (1987)). Other antibody-basedmethods useful for detecting protein gene expression includeimmunoassays, such as the enzyme linked immunosorbent assay (ELISA) andthe radioimmunoassay (RIA). Suitable antibody assay labels are known inthe art and include enzyme labels, such as, glucose oxidase;radioisotopes, such as iodine (125I, 121I), carbon (14C), sulfur (35S),tritium (3H), indium (112In), and technetium (99Tc); luminescent labels,such as luminol; and fluorescent labels, such as fluorescein andrhodamine, and biotin.

One facet of the invention is the detection and diagnosis of a diseaseor disorder associated with aberrant expression of a Therapeutic proteinin an animal, preferably a mammal and most preferably a human. In oneembodiment, diagnosis comprises: a) administering (for example,parenterally, subcutaneously, or intraperitoneally) to a subject aneffective amount of a labeled molecule which specifically binds to thepolypeptide of interest; b) waiting for a time interval following theadministering for permitting the labeled molecule to preferentiallyconcentrate at sites in the subject where the Therapeutic protein isexpressed (and for unbound labeled molecule to be cleared to backgroundlevel); c) determining background level; and d) detecting the labeledmolecule in the subject, such that detection of labeled molecule abovethe background level indicates that the subject has a particular diseaseor disorder associated with aberrant expression of the therapeuticprotein. Background level can be determined by various methodsincluding, comparing the amount of labeled molecule detected to astandard value previously determined for a particular system.

It will be understood in the art that the size of the subject and theimaging system used will determine the quantity of imaging moiety neededto produce diagnostic images. In the case of a radioisotope moiety, fora human subject, the quantity of radioactivity injected will normallyrange from about 5 to 20 millicuries of 99mTc. The labeled antibody,antibody fragment, or albumin fusion protein comprising at least afragment or variant of an antibody that binds a Therapeutic protein willthen preferentially accumulate at the location of cells which containthe specific Therapeutic protein. In vivo tumor imaging is described inS. W. Burchiel et al., “Immunopharmacokinetics of RadiolabeledAntibodies and Their Fragments.” (Chapter 13 in Tumor Imaging: TheRadiochemical Detection of Cancer, S. W. Burchiel and B. A. Rhodes,eds., Masson Publishing Inc. (1982)).

Depending on several variables, including the type of label used and themode of administration, the time interval following the administrationfor permitting the labeled molecule to preferentially concentrate atsites in the subject and for unbound labeled molecule to be cleared tobackground level is 6 to 48 hours or 6 to 24 hours or 6 to 12 hours. Inanother embodiment the time interval following administration is 5 to 20days or 5 to 10 days.

In an embodiment, monitoring of the disease or disorder is carried outby repeating the method for diagnosing the disease or disease, forexample, one month after initial diagnosis, six months after initialdiagnosis, one year after initial diagnosis, etc.

Presence of the labeled molecule can be detected in the patient usingmethods known in the art for in vivo scanning. These methods depend uponthe type of label used. Skilled artisans will be able to determine theappropriate method for detecting a particular label. Methods and devicesthat may be used in the diagnostic methods of the invention include, butare not limited to, computed tomography (CT), whole body scan such asposition emission tomography (PET), magnetic resonance imaging (MRI),and sonography.

In a specific embodiment, the molecule is labeled with a radioisotopeand is detected in the patient using a radiation responsive surgicalinstrument (Thurston et al., U.S. Pat. No. 5,441,050). In anotherembodiment, the molecule is labeled with a fluorescent compound and isdetected in the patient using a fluorescence responsive scanninginstrument. In another embodiment, the molecule is labeled with apositron emitting metal and is detected in the patent using positronemission-tomography. In yet another embodiment, the molecule is labeledwith a paramagnetic label and is detected in a patient using magneticresonance imaging (MRI). Antibodies that specifically detect the albuminfusion protein but not albumin or the therapeutic protein alone are apreferred embodiment. These can be used to detect the albumin fusionprotein as described throughout the specification.

Kits

The present invention provides kits that can be used in the abovemethods. In one embodiment, a kit comprises an antibody, preferably apurified antibody, in one or more containers. In a specific embodiment,the kits of the present invention contain a substantially isolatedpolypeptide comprising an epitope which is specifically immunoreactivewith an antibody included in the kit. Preferably, the kits of thepresent invention further comprise a control antibody which does notreact with the polypeptide of interest. In another specific embodiment,the kits of the present invention contain a means for detecting thebinding of an antibody to a polypeptide of interest (e.g., the antibodymay be conjugated to a detectable substrate such as a fluorescentcompound, an enzymatic substrate, a radioactive compound or aluminescent compound, or a second antibody which recognizes the firstantibody may be conjugated to a detectable substrate).

In another specific embodiment of the present invention, the kit is adiagnostic kit for use in screening serum containing antibodies specificagainst proliferative and/or cancerous polynucleotides and polypeptides.Such a kit may include a control antibody that does not react with thepolypeptide of interest. Such a kit may include a substantially isolatedpolypeptide antigen comprising an epitope which is specificallyimmunoreactive with at least one anti-polypeptide antigen antibody.Further, such a kit includes means for detecting the binding of saidantibody to the antigen (e.g., the antibody may be conjugated to afluorescent compound such as fluorescein or rhodamine which can bedetected by flow cytometry). In specific embodiments, the kit mayinclude a recombinantly produced or chemically synthesized polypeptideantigen. The polypeptide antigen of the kit may also be attached to asolid support.

In a more specific embodiment the detecting means of the above-describedkit includes a solid support to which said polypeptide antigen isattached. Such a kit may also include a non-attached reporter-labeledanti-human antibody. In this embodiment, binding of the antibody to thepolypeptide antigen can be detected by binding of the saidreporter-labeled antibody.

In an additional embodiment, the invention includes a diagnostic kit foruse in screening serum containing antigens of the polypeptide of theinvention. The diagnostic kit includes a substantially isolated antibodyspecifically immunoreactive with polypeptide or polynucleotide antigens,and means for detecting the binding of the polynucleotide or polypeptideantigen to the antibody. In one embodiment, the antibody is attached toa solid support. In a specific embodiment, the antibody may be amonoclonal antibody. The detecting means of the kit may include asecond, labeled monoclonal antibody. Alternatively, or in addition, thedetecting means may include a labeled, competing antigen.

In one diagnostic configuration, test serum is reacted with a solidphase reagent having a surface-bound antigen obtained by the methods ofthe present invention. After binding with specific antigen antibody tothe reagent and removing unbound serum components by washing, thereagent is reacted with reporter-labeled anti-human antibody to bindreporter to the reagent in proportion to the amount of boundanti-antigen antibody on the solid support. The reagent is again washedto remove unbound labeled antibody, and the amount of reporterassociated with the reagent is determined. Typically, the reporter is anenzyme which is detected by incubating the solid phase in the presenceof a suitable fluorometric, luminescent or colorimetric substrate(Sigma, St. Louis, Mo.).

The solid surface reagent in the above assay is prepared by knowntechniques for attaching protein material to solid support material,such as polymeric beads, dip sticks, 96-well plate or filter material.These attachment methods generally include non-specific adsorption ofthe protein to the support or covalent attachment of the protein,typically through a free amine group, to a chemically reactive group onthe solid support, such as an activated carboxyl, hydroxyl, or aldehydegroup. Alternatively, streptavidin coated plates can be used inconjunction with biotinylated antigen(s).

Thus, the invention provides an assay system or kit for carrying outthis diagnostic method. The kit generally includes a support withsurface-bound recombinant antigens, and a reporter-labeled anti-humanantibody for detecting surface-bound anti-antigen antibody.

Albumin Fusion Proteins

The present invention relates generally to albumin fusion proteins andmethods of treating, preventing, or ameliorating diseases or disorders.As used herein, “albumin fusion protein” refers to a protein formed bythe fusion of at least one molecule of albumin (or a fragment or variantthereof) to at least one molecule of a Therapeutic protein (or fragmentor variant thereof). An albumin fusion protein of the inventioncomprises at least a fragment or variant of a Therapeutic protein and atleast a fragment or variant of human serum albumin, which are associatedwith one another, preferably by genetic fusion (i.e., the albumin fusionprotein is generated by translation of a nucleic acid in which apolynucleotide encoding all or a portion of a Therapeutic protein isjoined in-frame with a polynucleotide encoding all or a portion ofalbumin) or to one another. The Therapeutic protein and albumin protein,once part of the albumin fusion protein, may each be referred to as a“portion”, “region” or “moiety” of the albumin fusion protein.

In a preferred embodiment, the invention provides an albumin fusionprotein encoded by a polynucleotide or albumin fusion constructdescribed in Table 1 or Table 2. Polynucleotides encoding these albuminfusion proteins are also encompassed by the invention.

Preferred albumin fusion proteins of the invention, include, but are notlimited to, albumin fusion proteins encoded by a nucleic acid moleculecomprising, or alternatively consisting of, a polynucleotide encoding atleast one molecule of albumin (or a fragment or variant thereof) joinedin frame to at least one polynucleotide encoding at least one moleculeof a Therapeutic protein (or fragment or variant thereof); a nucleicacid molecule comprising, or alternatively consisting of, apolynucleotide encoding at least one molecule of albumin (or a fragmentor variant thereof) joined in frame to at least one polynucleotideencoding at least one molecule of a Therapeutic protein (or fragment orvariant thereof) generated as described in Table 1, Table 2 or in theExamples; or a nucleic acid molecule comprising, or alternativelyconsisting of, a polynucleotide encoding at least one molecule ofalbumin (or a fragment or variant thereof) joined in frame to at leastone polynucleotide encoding at least one molecule of a Therapeuticprotein (or fragment or variant thereof), further comprising, forexample, one or more of the following elements: (1) a functionalself-replicating vector (including but not limited to, a shuttle vector,an expression vector, an integration vector, and/or a replicationsystem), (2) a region for initiation of transcription (e.g., a promoterregion, such as for example, a regulatable or inducible promoter, aconstitutive promoter), (3) a region for termination of transcription,(4) a leader sequence, and (5) a selectable marker.

In one embodiment, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a Therapeutic protein (e.g.,as described in Table 1) and a serum albumin protein. In otherembodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a biologically active and/ortherapeutically active fragment of a Therapeutic protein and a serumalbumin protein. In other embodiments, the invention provides an albuminfusion protein comprising, or alternatively consisting of, abiologically active and/or therapeutically active variant of aTherapeutic protein and a serum albumin protein. In preferredembodiments, the serum albumin protein component of the albumin fusionprotein is the mature portion of serum albumin.

In further embodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a Therapeutic protein, and abiologically active and/or therapeutically active fragment of serumalbumin. In further embodiments, the invention provides an albuminfusion protein comprising, or alternatively consisting of, a Therapeuticprotein and a biologically active and/or therapeutically active variantof serum albumin. In preferred embodiments, the Therapeutic proteinportion of the albumin fusion protein is the mature portion of theTherapeutic protein.

In further embodiments, the invention provides an albumin fusion proteincomprising, or alternatively consisting of, a biologically active and/ortherapeutically active fragment or variant of a Therapeutic protein anda biologically active and/or therapeutically active fragment or variantof serum albumin. In preferred embodiments, the invention provides analbumin fusion protein comprising, or alternatively consisting of, themature portion of a Therapeutic protein and the mature portion of serumalbumin.

Preferably, the albumin fusion protein comprises HA as the N-terminalportion, and a Therapeutic protein as the C-terminal portion.Alternatively, an albumin fusion protein comprising HA as the C-terminalportion, and a Therapeutic protein as the N-terminal portion may also beused.

In other embodiments, the albumin fusion protein has a Therapeuticprotein fused to both the N-terminus and the C-terminus of albumin. In apreferred embodiment, the Therapeutic proteins fused at the N- andC-termini are the same Therapeutic proteins. In an alternative preferredembodiment, the Therapeutic proteins fused at the N- and C-termini aredifferent Therapeutic proteins. In another preferred embodiment, theTherapeutic proteins fused at the N- and C-termini are differentTherapeutic proteins which may be used to treat or prevent the same or arelated disease, disorder, or condition (e.g. as listed in the“Preferred Indication Y” column of Table 1). In another preferredembodiment, the Therapeutic proteins fused at the N- and C-termini aredifferent Therapeutic proteins which may be used to treat, ameliorate,or prevent diseases or disorders (e.g. as listed in the “PreferredIndication Y” column of Table 1) which are known in the art to commonlyoccur in patients simultaneously, concurrently, or consecutively, orwhich commonly occur in patients in association with one another.

Exemplary fusion proteins of the invention containing multipleTherapeutic protein portions fused at the N- and C-termini of albumininclude, but are not limited to, GCSF-HSA-EPO, EPO-HSA-GCSF,IFNalpha-HSA-IL2, IL2-HSA-IFNalpha, GCSF-HSA-IL2, IL2-HSA-GCSF,IL2-HSA-EPO, EPO-HSA-IL2, IL3-HSA-EPO, EPO-HSA-IL3, GCSF-HSA-GMCSF,GMCSF-HSA-GCSF, IL2-HSA-GMCSF, GMCSF-HSA-IL2, PTH-HSA-Calcitonin,Calcitonin-HSA-PTH, PTH-PTH-HSA-Calcitonin, Calcitonin-HSA-PTH-PTH,PTH-Calcitonin-HSA-PTH, or PTH-HSA-Calcitonin-PTH.

Albumin fusion proteins of the invention encompass proteins containingone, two, three, four, or more molecules of a given Therapeutic proteinX or variant thereof fused to the N- or C-terminus of an albumin fusionprotein of the invention, and/or to the N- and/or C-terminus of albuminor variant thereof. Molecules of a given Therapeutic protein X orvariants thereof may be in any number of orientations, including, butnot limited to, a ‘head to head’ orientation (e.g., wherein theN-terminus of one molecule of a Therapeutic protein X is fused to theN-terminus of another molecule of the Therapeutic protein X), or a ‘headto tail’ orientation (e.g., wherein the C-terminus of one molecule of aTherapeutic protein X is fused to the N-terminus of another molecule ofTherapeutic protein X).

In one embodiment, one, two, three, or more tandemly orientedTherapeutic protein X polypeptides (or fragments or variants thereof)are fused to the N- or C-terminus of an albumin fusion protein of theinvention, and/or to the N- and/or C-terminus of albumin or variantthereof.

In a specific embodiment, one, two, three, four, five, or more tandemlyoriented molecules of PTH are fused to the N- or C-terminus of albuminor variant thereof. For example, one, two, three, four, five, or moretandemly oriented molecules of PTH (including, but not limited to,molecules of PTH comprising, or alternatively consisting of, amino acids1 to 34) are fused to the N- or C-terminus of albumin or variantthereof. Exemplary fusion proteins of the invention containing multipleprotein portions of PTH, include, but are not limited to, PTH-PTH-HSA,HSA-PTH-PTH, PTH-PTH-PTH-HSA, HSA-PTH-PTH-PTH, PTH-PTH-PTH-PTH-HSA, orHSA-PTH-PTH-PTH-PTH.

In another specific embodiment, one, two, three, four, five, or moretandemly oriented molecules of GLP-1 are fused to the N- or C-terminusof albumin or variant thereof. For example, one, two, three, four, five,or more tandemly oriented molecules of GLP-1 (including, but not limitedto, molecules of GLP-1 comprising, or alternatively consisting of, aminoacids 7 to 36, with residue 8 being mutated from an Alanine to aGlycine) (See for Example, the mutants disclosed in U.S. Pat. No.5,545,618, herein incorporated by reference in its entirety) are fusedto the N- or C-terminus of albumin or variant thereof. Exemplary fusionproteins of the invention containing multiple protein portions of GLP-1,include, but are not limited to, GL1-GLP1-HSA, HSA-GLP1-GLP1,GLP1mutant-GLP1mutant-HSA, HSA-GLP1mutant-GLP1mutant,GLP1mutant-GLP1-HSA, HSA-GLP 1mutant-GLP 1, GLP1-GLP1mutant-HSA, orHSA-GLP1-GLP1mutant. Particularly preferred embodiments are GLP-1 tandemfusions such as construct ID #3070 and the protein encoded by suchconstruct.

Albumin fusion proteins of the invention further encompass proteinscontaining one, two, three, four, or more molecules of a givenTherapeutic protein X or variant thereof fused to the N- or C-terminusof an albumin fusion protein of the invention, and/or to the N- and/orC-terminus of albumin or variant thereof, wherein the molecules arejoined through peptide linkers. Examples include those peptide linkersdescribed in U.S. Pat. No. 5,073,627 (hereby incorporated by reference).Albumin fusion proteins comprising multiple Therapeutic protein Xpolypeptides separated by peptide linkers may be produced usingconventional recombinant DNA technology. Linkers are particularlyimportant when fusing a small peptide to the large HSA molecule. Thepeptide itself can be a linker by fusing tandem copies of the peptide(see for example GLP-1) or other known linkers can be used. Constructsthat incorporate linkers are described in Table 2 or are apparent whenexamining SEQ ID NO:Y.

Further, albumin fusion proteins of the invention may also be producedby fusing a Therapeutic protein X or variants thereof to the N-terminaland/or C-terminal of albumin or variants thereof in such a way as toallow the formation of intramolecular and/or intermolecular multimericforms. In one embodiment of the invention, albumin fusion proteins maybe in monomeric or multimeric forms (i.e., dimers, trimers, tetramersand higher multimers). In a further embodiment of the invention, theTherapeutic protein portion of an albumin fusion protein may be inmonomeric form or multimeric form (i.e., dimers, trimers, tetramers andhigher multimers). In a specific embodiment, the Therapeutic proteinportion of an albumin fusion protein is in multimeric form (i.e.,dimers, trimers, tetramers and higher multimers), and the albuminprotein portion is in monomeric form.

In addition to albumin fusion protein in which the albumin portion isfused N-terminal and/or C-terminal of the Therapeutic protein portion,albumin fusion proteins of the invention may also be produced byinserting the Therapeutic protein or peptide of interest (e.g., aTherapeutic protein X as disclosed in Table 1, or an antibody that bindsa Therapeutic protein or a fragment or variant thereof) into an internalregion of HA. For instance, within the protein sequence of the HAmolecule a number of loops or turns exist between the end and beginningof a-helices, which are stabilized by disulphide bonds. The loops, asdetermined from the crystal structure of HA (PDB identifiers 1AO6, 1BJ5,1BKE, 1BM0, 1E7E to 1E7I and 1UOR) for the most part extend away fromthe body of the molecule. These loops are useful for the insertion, orinternal fusion, of therapeutically active peptides, particularly thoserequiring a secondary structure to be functional, or Therapeuticproteins, to essentially generate an albumin molecule with specificbiological activity.

Loops in human albumin structure into which peptides or polypeptides maybe inserted to generate albumin fusion proteins of the inventioninclude: Val54-Asn61, Thr76-Asp89, Ala92-Glu100, Gln170-Ala176, His247-Glu252, Glu 266-Glu277, Glu 280-His288, Ala362-Glu368,Lys439-Pro447, Val462-Lys475, Thr478-Pro486, and Lys560-Thr566. In morepreferred embodiments, peptides or polypeptides are inserted into theVal54-Asn61, Gln170-Ala176, and/or Lys560-Thr566 loops of mature humanalbumin (SEQ ID NO:1038).

Peptides to be inserted may be derived from either phage display orsynthetic peptide libraries screened for specific biological activity orfrom the active portions of a molecule with the desired function.Additionally, random peptide libraries may be generated withinparticular loops or by insertions of randomized peptides into particularloops of the HA molecule and in which all possible combinations of aminoacids are represented.

Such library(s) could be generated on HA or domain fragments of HA byone of the following methods:

randomized mutation of amino acids within one or more peptide loops ofHA or HA domain fragments. Either one, more or all the residues within aloop could be mutated in this manner;

replacement of, or insertion into one or more loops of HA or HA domainfragments (i.e., internal fusion) of a randomized peptide(s) of lengthX_(n) (where X is an amino acid and n is the number of residues;

N-, C- or N- and C-terminal peptide/protein fusions in addition to (a)and/or (b).

The HA or HA domain fragment may also be made multifunctional bygrafting the peptides derived from different screens of different loopsagainst different targets into the same HA or HA domain fragment.

In preferred embodiments, peptides inserted into a loop of human serumalbumin are peptide fragments or peptide variants of the Therapeuticproteins disclosed in Table 1. More particularly, the inventionencompasses albumin fusion proteins which comprise peptide fragments orpeptide variants at least 7 at least 8, at least 9, at least 10, atleast 11, at least 12, at least 13, at least 14, at least 15, at least20, at least 25, at least 30, at least 35, or at least 40 amino acids inlength inserted into a loop of human serum albumin. The invention alsoencompasses albumin fusion proteins which comprise peptide fragments orpeptide variants at least 7 at least 8, at least 9, at least 10, atleast 11, at least 12, at least 13, at least 14, at least 15, at least20, at least 25, at least 30, at least 35, or at least 40 amino acidsfused to the N-terminus of human serum albumin. The invention alsoencompasses albumin fusion proteins which comprise peptide fragments orpeptide variants at least 7 at least 8, at least 9, at least 10, atleast 11, at least 12, at least 13, at least 14, at least 15, at least20, at least 25, at least 30, at least 35, or at least 40 amino acidsfused to the C-terminus of human serum albumin. For example, shortpeptides described in Table 1 and 2 (e.g., Therapeutic Y) can beinserted into the albumin loops.

Generally, the albumin fusion proteins of the invention may have oneHA-derived region and one Therapeutic protein-derived region. Multipleregions of each protein, however, may be used to make an albumin fusionprotein of the invention. Similarly, more than one Therapeutic proteinmay be used to make an albumin fusion protein of the invention. Forinstance, a Therapeutic protein may be fused to both the N- andC-terminal ends of the HA. In such a configuration, the Therapeuticprotein portions may be the same or different Therapeutic proteinmolecules. The structure of bifunctional albumin fusion proteins may berepresented as: X-HA-Y or Y-HA-X.

For example, an anti-BLyS™ scFv-HA-IFNα-2b fusion may be prepared tomodulate the immune response to IFNα-2b by anti-BLyS™ scFv. Analternative is making a bi (or even multi) functional dose of HA-fusionse.g. HA-IFNα-2b fusion mixed with HA-anti-BLyS™ scFv fusion or otherHA-fusions in various ratio's depending on function, half-life etc.

Bi- or multi-functional albumin fusion proteins may also be prepared totarget the Therapeutic protein portion of a fusion to a target organ orcell type via protein or peptide at the opposite terminus of HA.

As an alternative to the fusion of known therapeutic molecules, thepeptides could be obtained by screening libraries constructed as fusionsto the N-, C- or N- and C-termini of HA, or domain fragment of HA, oftypically 6, 8, 12, 20 or 25 or X_(n) (where X is an amino acid (aa) andn equals the number of residues) randomized amino acids, and in whichall possible combinations of amino acids were represented. A particularadvantage of this approach is that the peptides may be selected in situon the HA molecule and the properties of the peptide would therefore beas selected for rather than, potentially, modified as might be the casefor a peptide derived by any other method then being attached to HA.

Additionally, the albumin fusion proteins of the invention may include alinker peptide between the fused portions to provide greater physicalseparation between the moieties and thus maximize the accessibility ofthe Therapeutic protein portion, for instance, for binding to itscognate receptor. The linker peptide may consist of amino acids suchthat it is flexible or more rigid.

The linker sequence may be cleavable by a protease or chemically toyield the growth hormone related moiety. Preferably, the protease is onewhich is produced naturally by the host, for example the S. cerevisiaeprotease kex2 or equivalent proteases.

Therefore, as described above, the albumin fusion proteins of theinvention may have the following formula R1-L-R2; R2-L-R1; orR1-L-R2-L-R1, wherein R1 is at least one Therapeutic protein, peptide orpolypeptide sequence, and not necessarily the same Therapeutic protein,L is a linker and R2 is a serum albumin sequence.

In preferred embodiments, Albumin fusion proteins of the inventioncomprising a Therapeutic protein have extended shelf life compared tothe shelf life the same Therapeutic protein when not fused to albumin.Shelf-life typically refers to the time period over which thetherapeutic activity of a Therapeutic protein in solution or in someother storage formulation, is stable without undue loss of therapeuticactivity. Many of the Therapeutic proteins are highly labile in theirunfused state. As described below, the typical shelf-life of theseTherapeutic proteins is markedly prolonged upon incorporation into thealbumin fusion protein of the invention.

Albumin fusion proteins of the invention with “prolonged” or “extended”shelf-life exhibit greater therapeutic activity relative to a standardthat has been subjected to the same storage and handling conditions. Thestandard may be the unfused full-length Therapeutic protein. When theTherapeutic protein portion of the albumin fusion protein is an analog,a variant, or is otherwise altered or does not include the completesequence for that protein, the prolongation of therapeutic activity mayalternatively be compared to the unfused equivalent of that analog,variant, altered peptide or incomplete sequence. As an example, analbumin fusion protein of the invention may retain greater than about100% of the therapeutic activity, or greater than about 105%, 110%,120%, 130%, 150% or 200% of the therapeutic activity of a standard whensubjected to the same storage and handling conditions as the standardwhen compared at a given time point.

Shelf-life may also be assessed in terms of therapeutic activityremaining after storage, normalized to therapeutic activity when storagebegan. Albumin fusion proteins of the invention with prolonged orextended shelf-life as exhibited by prolonged or extended therapeuticactivity may retain greater than about 50% of the therapeutic activity,about 60%, 70%, 80%, or 90% or more of the therapeutic activity of theequivalent unfused Therapeutic protein when subjected to the sameconditions. For example, as discussed in Example 38, an albumin fusionprotein of the invention comprising hGH fused to the full length HAsequence may retain about 80% or more of its original activity insolution for periods of up to 5 weeks or more under various temperatureconditions.

Expression of Fusion Proteins

The albumin fusion proteins of the invention may be produced asrecombinant molecules by secretion from yeast, a microorganism such as abacterium, or a human or animal cell line. Preferably, the polypeptideis secreted from the host cells.

A particular embodiment of the invention comprises a DNA constructencoding a signal sequence effective for directing secretion in yeast,particularly a yeast-derived signal sequence (especially one which ishomologous to the yeast host), and the fused molecule of the firstaspect of the invention, there being no yeast-derived pro sequencebetween the signal and the mature polypeptide.

The Saccharomyces cerevisiae invertase signal is a preferred example ofa yeast-derived signal sequence.

Conjugates of the kind prepared by Poznansky et al., (FEBS Lett. 239:18(1988)), in which separately-prepared polypeptides are joined bychemical cross-linking, are not contemplated.

The present invention also includes a cell, preferably a yeast celltransformed to express an albumin fusion protein of the invention. Inaddition to the transformed host cells themselves, the present inventionalso contemplates a culture of those cells, preferably a monoclonal(clonally homogeneous) culture, or a culture derived from a monoclonalculture, in a nutrient medium. If the polypeptide is secreted, themedium will contain the polypeptide, with the cells, or without thecells if they have been filtered or centrifuged away. Many expressionsystems are known and may be used, including bacteria (for example E.coli and Bacillus subtilis), yeasts (for example Saccharomycescerevisiae, Kluyveromyces lactis and Pichia pastoris, filamentous fungi(for example Aspergillus), plant cells, animal cells and insect cells.

Preferred yeast strains to be used in the production of albumin fusionproteins are D88, DXY1 and BXP10. D88 [leu2-3, leu2-122, can1, pra1,ubc4] is a derivative of parent strain AH22his⁺ (also known as DB1; see,e.g., Sleep et al. Biotechnology 8:42-46 (1990)). The strain contains aleu2 mutation which allows for auxotropic selection of 2 micron-basedplasmids that contain the LEU2 gene. D88 also exhibits a derepression ofPRB1 in glucose excess. The PRB1 promoter is normally controlled by twocheckpoints that monitor glucose levels and growth stage. The promoteris activated in wild type yeast upon glucose depletion and entry intostationary phase. Strain D88 exhibits the repression by glucose butmaintains the induction upon entry into stationary phase. The PRA1 geneencodes a yeast vacuolar protease, YscA endoprotease A, that islocalized in the ER. The UBC4 gene is in the ubiquitination pathway andis involved in targeting short lived and abnormal proteins for ubiquitindependant degradation. Isolation of this ubc4 mutation was found toincrease the copy number of an expression plasmid in the cell and causean increased level of expression of a desired protein expressed from theplasmid (see, e.g., International Publication No. WO99/00504, herebyincorporated in its entirety by reference herein).

DXY1, a derivative of D88, has the following genotype: [leu2-3,leu2-122, can1, pra1, ubc4, ura3::yap3]. In addition to the mutationsisolated in D88, this strain also has a knockout of the YAP3 protease.This protease causes cleavage of mostly di-basic residues (RR, RK, KR,KK) but can also promote cleavage at single basic residues in proteins.Isolation of this yap3 mutation resulted in higher levels of full lengthHSA production (see, e.g., U.S. Pat. No. 5,965,386 and Kerry-Williams etal., Yeast 14:161-169 (1998), hereby incorporated in their entireties byreference herein).

BXP10 has the following genotype: leu2-3, leu2-122, can1, pra1, ubc4,ura3, yap3::URA3, lys2, hsp150::LYS2, pmt1:URA3. In addition to themutations isolated in DXY1, this strain also has a knockout of the PMT1gene and the HSP150 gene. The PMT1 gene is a member of theevolutionarily conserved family of dolichyl-phosphate-D-mannose proteinO-mannosyltransferases (Pmts). The transmembrane topology of Pmt1psuggests that it is an integral membrane protein of the endoplasmicreticulum with a role in O-linked glycosylation. This mutation serves toreduce/eliminate O-linked glycosylation of HSA fusions (see, e.g.,International Publication No. WO00/44772, hereby incorporated in itsentirety by reference herein). Studies revealed that the Hsp150 proteinis inefficiently separated from rHA by ion exchange chromatography. Themutation in the HSP150 gene removes a potential contaminant that hasproven difficult to remove by standard purification techniques. See,e.g., U.S. Pat. No. 5,783,423, hereby incorporated in its entirety byreference herein.

The desired protein is produced in conventional ways, for example from acoding sequence inserted in the host chromosome or on a free plasmid.The yeasts are transformed with a coding sequence for the desiredprotein in any of the usual ways, for example electroporation. Methodsfor transformation of yeast by electroporation are disclosed in Becker &Guarente (1990) Methods Enzymol. 194, 182.

Successfully transformed cells, i.e., cells that contain a DNA constructof the present invention, can be identified by well known techniques.For example, cells resulting from the introduction of an expressionconstruct can be grown to produce the desired polypeptide. Cells can beharvested and lysed and their DNA content examined for the presence ofthe DNA using a method such as that described by Southern (1975) J. Mol.Biol. 98, 503 or Berent et al. (1985) Biotech. 3, 208. Alternatively,the presence of the protein in the supernatant can be detected usingantibodies.

Useful yeast plasmid vectors include pRS403-406 and pRS413-416 and aregenerally available from Stratagene Cloning Systems, La Jolla, Calif.92037, USA. Plasmids pRS403, pRS404, pRS405 and pRS406 are YeastIntegrating plasmids (YIps) and incorporate the yeast selectable markersHIS3, 7RP1, LEU2 and URA3. Plasmids pRS413-416 are Yeast Centromereplasmids (Ycps).

Preferred vectors for making albumin fusion proteins for expression inyeast include pPPC0005, pScCHSA, pScNHSA, and pC4:HSA which aredescribed in detail in Example 1. FIG. 2 shows a map of the pPPC0005plasmid that can be used as the base vector into which polynucleotidesencoding Therapeutic proteins may be cloned to form HA-fusions. Itcontains a PRB1 S. cerevisiae promoter (PRB1p), a Fusion leader sequence(FL), DNA encoding HA (rHA) and an ADH1 S. cerevisiae terminatorsequence. The sequence of the fusion leader sequence consists of thefirst 19 amino acids of the signal peptide of human serum albumin (SEQID NO:1094) and the last five amino acids of the mating factor alpha 1promoter (SLDKR, see EP-A-387 319 which is hereby incorporated byreference in its entirety).

The plasmids, pPPC0005, pScCHSA, pScNHSA, and pC4:HSA were deposited onApr. 11, 2001 at the American Type Culture Collection, 10801 UniversityBoulevard, Manassas, Va. 20110-2209 and given accession numbers ATCCPTA-3278, PTA-3276, PTA-3279, and PTA-3277, respectively. Another vectoruseful for expressing an albumin fusion protein in yeast the pSAC35vector which is described in Sleep et al., BioTechnology 8:42 (1990)which is hereby incorporated by reference in its entirety.

Another yeast promoter that can be used to express the albumin fusionprotein is the MET25 promoter. See, for example, Dominik Mumburg, RolfMuller and Martin Funk. Nucleic Acids Research, 1994, Vol. 22, No. 25,pp. 5767-5768. The Met25 promoter is 383 bases long (bases −382 to −1)and the genes expressed by this promoter are also known as Met15, Met17,and YLR303W. A preferred embodiment uses the sequence below, where, atthe 5′ end of the sequence below, the Not 1 site used in the cloning isunderlined and at the 3′ end, the ATG start codon is underlined:

(SEQ ID NO: 2138) GCGGCCGCCGGATGCAAGGGTTCGAATCCCTTAGCTCTCATTATTTTTTGCTTTTTCTCTTGAGGTCACATGATCGCAAAATGGCAAATGGCACGTGAAGCTGTCGATATTGGGGAACTGTGGTGGTTGGCAAATGACTAATTAAGTTAGTCAAGGCGCCATCCTCATGAAAACTGTGTAACATAATAACCGAAGTGTCGAAAAGGTGGCACCTTGTCCAATTGAACACGCTCGATGAAAAAAATAAGATATATATAAGGTTAAGTAAAGCGTCTGTTAGAAAGGAAGTTTTTCCTTTTTCTTGCTCTCTTGTCTTTTCATCTACTATTTCCTTCGTGTAATACAGGGTCGTCAGATACATAGATACAATTCTATTACCCCCATCCATACAATG

A variety of methods have been developed to operably link DNA to vectorsvia complementary cohesive termini. For instance, complementaryhomopolymer tracts can be added to the DNA segment to be inserted to thevector DNA. The vector and DNA segment are then joined by hydrogenbonding between the complementary homopolymeric tails to formrecombinant DNA molecules.

Synthetic linkers containing one or more restriction sites provide analternative method of joining the DNA segment to vectors. The DNAsegment, generated by endonuclease restriction digestion, is treatedwith bacteriophage T4 DNA polymerase or E. coli DNA polymerase I,enzymes that remove protruding, gamma-single-stranded termini with their3′ 5′-exonucleolytic activities, and fill in recessed 3′-ends with theirpolymerizing activities.

The combination of these activities therefore generates blunt-ended DNAsegments. The blunt-ended segments are then incubated with a large molarexcess of linker molecules in the presence of an enzyme that is able tocatalyze the ligation of blunt-ended DNA molecules, such asbacteriophage T4 DNA ligase. Thus, the products of the reaction are DNAsegments carrying polymeric linker sequences at their ends. These DNAsegments are then cleaved with the appropriate restriction enzyme andligated to an expression vector that has been cleaved with an enzymethat produces termini compatible with those of the DNA segment.

Synthetic linkers containing a variety of restriction endonuclease sitesare commercially available from a number of sources includingInternational Biotechnologies Inc, New Haven, Conn., USA.

A desirable way to modify the DNA in accordance with the invention, if,for example, HA variants are to be prepared, is to use the polymerasechain reaction as disclosed by Saiki et al. (1988) Science 239, 487-491.In this method the DNA to be enzymatically amplified is flanked by twospecific oligonucleotide primers which themselves become incorporatedinto the amplified DNA. The specific primers may contain restrictionendonuclease recognition sites which can be used for cloning intoexpression vectors using methods known in the art.

Exemplary genera of yeast contemplated to be useful in the practice ofthe present invention as hosts for expressing the albumin fusionproteins are Pichia (Hansenula), Saccharomyces, Kluyveromyces, Candida,Torulopsis, Torulaspora, Schizosaccharomyces, Citeromyces, Pachysolen,Debaromyces, Metschunikowia, Rhodosporidium, Leucosporidium,Botryoascus, Sporidiobolus, Endomycopsis, and the like. Preferred generaare those selected from the group consisting of Saccharomyces,Schizosaccharomyces, Kluyveromyces, Pichia and Torulaspora. Examples ofSaccharomyces spp. are S. cerevisiae, S. italicus and S. rouxii.

Examples of Kluyveromyces spp. are K. fragilis, K. lactis and K.marxianus. A suitable Torulaspora species is T. delbrueckii. Examples ofPichia (Hansenula) spp. are P. angusta (formerly H. polymorpha), P.anomala (formerly H. anomala) and P. pastoris. Methods for thetransformation of S. cerevisiae are taught generally in EP 251 744, EP258 067 and WO 90/01063, all of which are incorporated herein byreference.

Preferred exemplary species of Saccharomyces include S. cerevisiae, S.italicus, S. diastaticus, and Zygosaccharomyces rouxii. Preferredexemplary species of Kluyveromyces include K. fragilis and K. lactis.Preferred exemplary species of Hansenula include H. polymorpha (nowPichia angusta), H. anomala (now Pichia anomala), and Pichia capsulata.Additional preferred exemplary species of Pichia include P. pastoris.Preferred exemplary species of Aspergillus include A. niger and A.nidulans. Preferred exemplary species of Yarrowia include Y. lipolytica.Many preferred yeast species are available from the ATCC. For example,the following preferred yeast species are available from the ATCC andare useful in the expression of albumin fusion proteins: Saccharomycescerevisiae Hansen, teleomorph strain BY4743 yap3 mutant (ATCC AccessionNo. 4022731); Saccharomyces cerevisiae Hansen, teleomorph strain BY4743hsp150 mutant (ATCC Accession No. 4021266); Saccharomyces cerevisiaeHansen, teleomorph strain BY4743 pmt1 mutant (ATCC Accession No.4023792); Saccharomyces cerevisiae Hansen, teleomorph (ATCC AccessionNos. 20626; 44773; 44774; and 62995); Saccharomyces diastaticus Andrewset Gilliland ex van der Walt, teleomorph (ATCC Accession No. 62987);Kluyveromyces lactis (Dombrowski) van der Walt, teleomorph (ATCCAccession No. 76492); Pichia angusta (Teunisson et al.) Kurtzman,teleomorph deposited as Hansenula polymorpha de Morais et Maia,teleomorph (ATCC Accession No. 26012); Aspergillus niger van Tieghem,anamorph (ATCC Accession No. 9029); Aspergillus niger van Tieghem,anamorph (ATCC Accession No. 16404); Aspergillus nidulans (Eidam)Winter, anamorph (ATCC Accession No. 48756); and Yarrowia lipolytica(Wickerham et al.) van der Walt et von Arx, teleomorph (ATCC AccessionNo. 201847).

Suitable promoters for S. cerevisiae include those associated with thePGKI gene, GAL1 or GAL10 genes, CYCI, PHO5, TRPI, ADHI, ADH2, the genesfor glyceraldehyde-3-phosphate dehydrogenase, hexokinase, pyruvatedecarboxylase, phosphofructokinase, triose phosphate isomerase,phosphoglucose isomerase, glucokinase, alpha-mating factor pheromone, [amating factor pheromone], the PRBI promoter, the GUT2 promoter, the GPDIpromoter, and hybrid promoters involving hybrids of parts of 5′regulatory regions with parts of 5′ regulatory regions of otherpromoters or with upstream activation sites (e.g. the promoter ofEP-A-258 067).

Convenient regulatable promoters for use in Schizosaccharomyces pombeare the thiamine-repressible promoter from the nmt gene as described byMaundrell (1990) J. Biol. Chem. 265, 10857-10864 and the glucoserepressible jbpl gene promoter as described by Hoffman & Winston (1990)Genetics 124, 807-816.

Methods of transforming Pichia for expression of foreign genes aretaught in, for example, Cregg et al. (1993), and various Phillipspatents (e.g. U.S. Pat. No. 4,857,467, incorporated herein byreference), and Pichia expression kits are commercially available fromInvitrogen BV, Leek, Netherlands, and Invitrogen Corp., San Diego,Calif. Suitable promoters include AOXI and AOX2. Gleeson et al. (1986)J. Gen. Microbiol. 132, 3459-3465 include information on Hansenulavectors and transformation, suitable promoters being MOX1 and FMD1;whilst EP 361 991, Fleer et al. (1991) and other-publications fromRhone-Poulenc Rorer teach how to express foreign proteins inKluyveromyces spp., a suitable promoter being PGKI.

The transcription termination signal is preferably the 3′ flankingsequence of a eukaryotic gene which contains proper signals fortranscription termination and polyadenylation. Suitable 3′ flankingsequences may, for example, be those of the gene naturally linked to theexpression control sequence used, i.e. may correspond to the promoter.Alternatively, they may be different in which case the terminationsignal of the S. cerevisiae ADHI gene is preferred.

The desired albumin fusion protein may be initially expressed with asecretion leader sequence, which may be any leader effective in theyeast chosen. Leaders useful in yeast include any of the following:

-   -   a) the MPIF-1 signal sequence (e.g., amino acids 1-21 of GenBank        Accession number AAB51134) MKVSVAALSCLMLVTALGSQA (SEQ ID        NO:2132)    -   b) the stanniocalcin signal sequence (MLQNSAVLLLLVISASA, SEQ ID        NO:1054)    -   c) the pre-pro region of the HSA signal sequence (e.g.,        MKWVTFISLLFLFSSAYSRGVFRR, SEQ ID NO:1176)    -   d) the pre region of the HSA signal sequence (e.g.,        MKWVTFISLLFLFSSAYS, SEQ ID NO:1177) or variants thereof, such        as, for example, MKWVSFISLLFLFSSAYS, (SEQ ID NO:1168)    -   e) the invertase signal sequence (e.g., MLLQAFLFLLAGFAAKISA, SEQ        ID NO:1108)    -   f) the yeast mating factor alpha signal sequence (e.g.,        MRFPSIFTAVLAFAASSALAAPVNTTTEDETAQIPAEAVIGYSDLEGDFDV        AVLPFSNSTNNGLLFINTTIASIAAKEEGVSLEKR, SEQ ID NO:1109 or        MRFPSIFTAVLAFAASSALAAPVNTTTEDETAQIPAEAVIGYSDLEGDFDV        AVLPFSNSTNNGLLFINTTIASIAAKEEGVSLDKR, SEQ ID NO:1109)    -   g) K. lactis killer toxin leader sequence    -   h) a hybrid signal sequence (e.g., MKWVSFISLLFLFSSAYSRSLEKR, SEQ        ID NO:1110)    -   i) an HSA/1MFα-1 hybrid signal sequence (also known as HSA/kex2)        (e.g., MKWVSFISLLFLFSSAYSRSLDKR, SEQ ID NO:1111)    -   j) a K. lactis killer/MFα-1 fusion leader sequence (e.g.,        MNIFYIFLFLLSFVQGSLDKR, SEQ ID NO:1169)    -   k) the Immunoglobulin Ig signal sequence (e.g.,        MGWSCIILFLVATATGVHS, SEQ ID NO:1095)    -   l) the Fibulin B precursor signal sequence (e.g.,        MERAAPSRRVPLPLLLLGGLALLAAGVDA, SEQ ID NO:1096)    -   m) the clusterin precursor signal sequence (e.g.,        MMKTLLLFVGLLLTWESGQVLG, SEQ ID NO:1097)    -   n) the insulin-like growth factor-binding protein 4 signal        sequence (e.g., MLPLCLVAALLLAAGPGPSLG, SEQ ID NO:1098)    -   o) variants of the pre-pro-region of the HSA signal sequence        such as, for example, MKWVSFISLLFLFSSAYSRGVFRR (SEQ ID NO:1167),        MKWVTFISLLFLFAGVLG (SEQ ID NO:1099), MKWVTFISLLFLFSGVLG (SEQ ID        NO:1100), MKWVTFISLLFLFGGVLG (SEQ ID NO:1101),        -   Modified HSA leader HSA #64 MKWVTFISLLFLFAGVSG (SEQ ID            NO:2133);        -   Modified HSA leader HSA #66 MKWVTFISLLFLFGGVSG (SEQ ID            NO:2134);        -   Modified HSA (A14) leader—MKWVTFISLLFLFAGVSG (SEQ ID NO:            1102);        -   Modified HSA (S 14) leader (also known as modified HSA            #65)—MKWVTFISLLFLFSGVSG (SEQ ID NO:1103),        -   Modified HSA (G14) leader—MKWVTFISLLFLFGGVSG (SEQ ID            NO:1104), or MKWVTFISLLFLFGGVLGDLHKS (SEQ ID NO:1105)    -   p) a consensus signal sequence (MPTWAWWLFLVLLLALWAPARG, SEQ ID        NO:1055)    -   q) acid phosphatase (PH05) leader (e.g., MFKSVVYSILAASLANA SEQ        ID NO:2135)    -   r) the pre-sequence of MFoz-1    -   s) the pre-sequence of 0 glucanase (BGL2)    -   t) killer toxin leader    -   u) the presequence of killer toxin    -   v) K. lactis killer toxin prepro (29 amino acids; 16 amino acids        of pre and 13 amino acids of pro) MNIFYIFLFLLSFVQGLEHTHRRGSLDKR        (SEQ ID NO:2136)    -   w) S. diastaticus glucoarnylase Il secretion leader sequence    -   x) S. carlsbergensis α-galactosidase (MEL1) secretion leader        sequence    -   y) Candida glucoarnylase leader sequence    -   z) The hybrid leaders disclosed in EP-A-387 319 (herein        incorporated by reference)    -   aa) the gp67 signal sequence (in conjunction with baculoviral        expression systems) (e.g., amino acids 1-19 of GenBank Accession        Number AAA72759) or    -   bb) the natural leader of the therapeutic protein X;    -   cc) S. cerevisiae invertase (SUC2) leader, as disclosed in JP        62-096086 (granted as 911036516, herein incorporate by        reference); or    -   dd) Inulinase—MKLAYSLLLPLAGVSASVINYKR (SEQ ID NO:2137).    -   ee) A modified TA57 propeptide leader variant        #1—MKLKTVRSAVLSSLFASQVLGQPIDDTESQTTSVNLMADDTESAFATQTN        SGGLDVVGLISMAKR (SEQ ID NO:2128)    -   ff) A modified TA57 propeptide leader variant        #2—MKLKTVRSAVLSSLFASQVLGQPIDDTESQTTSVNLMADDTESAFATQTN        SGGLDVVGLISMAEEGEPKR (SEQ ID NO:2129)

Additional Methods of Recombinant and Synthetic Production of AlbuminFusion Proteins

The present invention also relates to vectors containing apolynucleotide encoding an albumin fusion protein of the presentinvention, host cells, and the production of albumin fusion proteins bysynthetic and recombinant techniques. The vector may be, for example, aphage, plasmid, viral, or retroviral vector. Retroviral vectors may bereplication competent or replication defective. In the latter case,viral propagation generally will occur only in complementing host cells.

The polynucleotides encoding albumin fusion proteins of the inventionmay be joined to a vector containing a selectable marker for propagationin a host. Generally, a plasmid vector is introduced in a precipitate,such as a calcium phosphate precipitate, or in a complex with a chargedlipid. If the vector is a virus, it may be packaged in vitro using anappropriate packaging cell line and then transduced into host cells.

The polynucleotide insert should be operatively linked to an appropriatepromoter, such as the phage lambda PL promoter, the E. coli lac, trp,phoA and tac promoters, the SV40 early and late promoters and promotersof retroviral LTRs, to name a few. Other suitable promoters will beknown to the skilled artisan. The expression constructs will furthercontain sites for transcription initiation, termination, and, in thetranscribed region, a ribosome binding site for translation. The codingportion of the transcripts expressed by the constructs will preferablyinclude a translation initiating codon at the beginning and atermination codon (UAA, UGA or UAG) appropriately positioned at the endof the polypeptide to be translated.

As indicated, the expression vectors will preferably include at leastone selectable marker. Such markers include dihydrofolate reductase,G418, glutamine synthase, or neomycin resistance for eukaryotic cellculture, and tetracycline, kanamycin or ampicillin resistance genes forculturing in E. coli and other bacteria. Representative examples ofappropriate hosts include, but are not limited to, bacterial cells, suchas E. coli, Streptomyces and Salmonella typhimurium cells; fungal cells,such as yeast cells (e.g., Saccharomyces cerevisiae or Pichia pastoris(ATCC Accession No. 201178)); insect cells such as Drosophila S2 andSpodoptera 519 cells; animal cells such as CHO, COS, NSO, 293, and Bowesmelanoma cells; and plant cells. Appropriate culture mediums andconditions for the above-described host cells are known in the art.

Among vectors preferred for use in bacteria include pQE70, pQE60 andpQE-9, available from QIAGEN, Inc.; pBluescript vectors, Phagescriptvectors, pNH8A, pNH16a, pNH18A, pNH46A, available from StratageneCloning Systems, Inc.; and ptrc99a, pKK223-3, pKK233-3, pDR540, pRIT5available from Pharmacia Biotech, Inc. Among preferred eukaryoticvectors are pWLNEO, pSV2CAT, pOG44, pXT1 and pSG available fromStratagene; and pSVK3, pBPV, pMSG and pSVL available from Pharmacia.Preferred expression vectors for use in yeast systems include, but arenot limited to pYES2, pYD1, pTEF1/Zeo, pYES2/GS, pPICZ, pGAPZ,pGAPZalph, pPIC9, pPIC3.5, pHIL-D2, pHIL-S1, pPIC3.5K, pPIC9K, andPAO815 (all available from Invitrogen, Carlsbad, Calif.). Other suitablevectors will be readily apparent to the skilled artisan.

In one embodiment, polynucleotides encoding an albumin fusion protein ofthe invention may be fused to signal sequences which will direct thelocalization of a protein of the invention to particular compartments ofa prokaryotic or eukaryotic cell and/or direct the secretion of aprotein of the invention from a prokaryotic or eukaryotic cell. Forexample, in E. coli, one may wish to direct the expression of theprotein to the periplasmic space. Examples of signal sequences orproteins (or fragments thereof) to which the albumin fusion proteins ofthe invention may be fused in order to direct the expression of thepolypeptide to the periplasmic space of bacteria include, but are notlimited to, the pelB signal sequence, the maltose binding protein (MBP)signal sequence, MBP, the ompA signal sequence, the signal sequence ofthe periplasmic E. coli heat-labile enterotoxin B-subunit, and thesignal sequence of alkaline phosphatase. Several vectors arecommercially available for the construction of fusion proteins whichwill direct the localization of a protein, such as the pMAL series ofvectors (particularly the pMAL-p series) available from New EnglandBiolabs. In a specific embodiment, polynucleotides albumin fusionproteins of the invention may be fused to the pelB pectate lyase signalsequence to increase the efficiency of expression and purification ofsuch polypeptides in Gram-negative bacteria. See, U.S. Pat. Nos.5,576,195 and 5,846,818, the contents of which are herein incorporatedby reference in their entireties.

Examples of signal peptides that may be fused to an albumin fusionprotein of the invention in order to direct its secretion in mammaliancells include, but are not limited to:

-   -   a) the MPIF-1 signal sequence (e.g., amino acids 1-21 of GenBank        Accession number AAB51134) MKVSVAALSCLMLVTALGSQA (SEQ ID        NO:2132)    -   b) the stanniocalcin signal sequence (MLQNSAVLLLLVISASA, SEQ ID        NO:1054)    -   c) the pre-pro region of the HSA signal sequence (e.g.,        MKWVTFISLLFLFSSAYSRGVFRR, SEQ ID NO:1176)    -   d) the pre region of the HSA signal sequence (e.g.,        MKWVTFISLLFLFSSAYS, SEQ ID NO:1177) or variants thereof, such        as, for example, MKWVSFISLLFLFSSAYS, (SEQ ID NO:1168)    -   e) the invertase signal sequence (e.g., MLLQAFLFLLAGFAAKISA, SEQ        ID NO:1108)    -   f) the yeast mating factor alpha signal sequence (e.g.,        MRFPSIFTAVLAFAASSALAAPVNTTTEDETAQIPAEAVIGYSDLEGDFDVAVL        PFSNSTNNGLLFINTTIASIAAKEEGVSLEKR, SEQ ID NO:1109 or        MRFPSIFTAVLAFAASSALAAPVNTTTEDETAQIPAEAVIGYSDLEGDFDVAVL        PFSNSTNNGLLFINTTIASIAAKEEGVSLDKR, SEQ ID NO:1109)    -   g) K. lactis killer toxin leader sequence    -   h) a hybrid signal sequence (e.g., MKWVSFISLLFLFSSAYSRSLEKR, SEQ        ID NO:1110)    -   i) an HSA/MFα-1 hybrid signal sequence (also known as HSA/kex2)        (e.g., MKWVSFISLLFLFSSAYSRSLDKR, SEQ ID NO:1111)    -   j) a K. lactis killer/MFα-1 fusion leader sequence (e.g.,        MNIFYIFLFLLSFVQGSLDKR, SEQ ID NO:1169)    -   k) the Immunoglobulin Ig signal sequence (e.g.,        MGWSCIILFLVATATGVHS, SEQ ID NO:1095)    -   l) the Fibulin B precursor signal sequence (e.g.,        MERAAPSRRVPLPLLLLGGLALLAAGVDA, SEQ ID NO:1096)    -   m) the clusterin precursor signal sequence (e.g.,        MMKTLLLFVGLLLTWESGQVLG, SEQ ID NO:1097)    -   n) the insulin-like growth factor-binding protein 4 signal        sequence (e.g., MLPLCLVAALLLAAGPGPSLG, SEQ ID NO:1098)    -   o) variants of the pre-pro-region of the HSA signal sequence        such as, for example, MKWVSFISLLFLFSSAYSRGVFRR (SEQ ID NO:1167),        MKWVTFISLLFLFAGVLG (SEQ ID NO:1099), MKWVTFISLLFLFSGVLG (SEQ ID        NO:1100), MKWVTFISLLFLFGGVLG (SEQ ID NO:1101),        -   Modified HSA leader HSA #64 MKWVTFISLLFLFAGVSG (SEQ ID            NO:2133);        -   Modified HSA leader HSA #66 MKWVTFISLLFLFGGVSG (SEQ ID            NO:2134);        -   Modified HSA (A14) leader—MKWVTFISLLFLFAGVSG (SEQ ID NO:            1102);        -   Modified HSA (S14) leader (also known as modified HSA            #65)—MKWVTFISLLFLFSGVSG (SEQ ID NO:1103),

Modified HSA (G14) leader—MKWVTFISLLFLFGGVSG (SEQ ID NO:1104), orMKWVTFISLLFLFGGVLGDLHKS (SEQ ID NO:1105)

-   -   p) a consensus signal sequence (MPTWAWWLFLVLLLALWAPARG, SEQ ID        NO:1055)    -   q) acid phosphatase (PH05) leader (e.g., MFKSVVYSILAASLANA SEQ        ID NO:2135)    -   r) the pre-sequence of MFoz-1    -   s) the pre-sequence of 0 glucanase (BGL2)    -   t) killer toxin leader    -   u) the presequence of killer toxin    -   v) K. lactis killer toxin prepro (29 amino acids; 16 amino acids        of pre and 13 amino acids of pro) MNIFYIFLFLLSFVQGLEHTHRRGSLDKR        (SEQ ID NO:2136)    -   w) S. diastaticus glucoarnylase Il secretion leader sequence    -   x) S. carlsbergensis α-galactosidase (MEL1) secretion leader        sequence    -   y) Candida glucoarnylase leader sequence    -   z) The hybrid leaders disclosed in EP-A-387 319 (herein        incorporated by reference)    -   aa) the gp67 signal sequence (in conjunction with baculoviral        expression systems) (e.g., amino acids 1-19 of GenBank Accession        Number AAA72759) or    -   bb) the natural leader of the therapeutic protein X;    -   cc) S. cerevisiae invertase (SUC2) leader, as disclosed in JP        62-096086 (granted as 911036516, herein incorporate by        reference); or    -   dd) Inulinase—MKLAYSLLLPLAGVSASVINYKR (SEQ ID NO:2137).    -   ee) A modified TA57 propeptide leader variant        #1—MKLKTVRSAVLSSLFASQVLGQPIDDTESQTTSVNLMADDTESAFATQTNSGG        LDVVGLISMAKR (SEQ ID NO:2128)    -   ff) A modified TA57 propeptide leader variant        #2—MKLKTVRSAVLSSLFASQVLGQPIDDTESQTTSVNLMADDTESAFATQTNSG        GLDVVGLISMAEEGEPKR (SEQ ID NO:2129)

Vectors which use glutamine synthase (GS) or DHFR as the selectablemarkers can be amplified in the presence of the drugs methioninesulphoximine or methotrexate, respectively. An advantage of glutaminesynthase based vectors are the availability of cell lines (e.g., themurine myeloma cell line, NSO) which are glutamine synthase negative.Glutamine synthase expression systems can also function in glutaminesynthase expressing cells (e.g., Chinese Hamster Ovary (CHO) cells) byproviding additional inhibitor to prevent the functioning of theendogenous gene. A glutamine synthase expression system and componentsthereof are detailed in PCT publications: WO87/04462; WO86/05807;WO89/01036; WO89/10404; and WO91/06657, which are hereby incorporated intheir entireties by reference herein. Additionally, glutamine synthaseexpression vectors can be obtained from Lonza Biologics, Inc.(Portsmouth, N.H.). Expression and production of monoclonal antibodiesusing a GS expression system in murine myeloma cells is described inBebbington et al., Bio/technology 10:169 (1992) and in Biblia andRobinson Biotechnol. Prog. 11:1 (1995) which are herein incorporated byreference.

The present invention also relates to host cells containing theabove-described vector constructs described herein, and additionallyencompasses host cells containing nucleotide sequences of the inventionthat are operably associated with one or more heterologous controlregions (e.g., promoter and/or enhancer) using techniques known of inthe art. The host cell can be a higher eukaryotic cell, such as amammalian cell (e.g., a human derived cell), or a lower eukaryotic cell,such as a yeast cell, or the host cell can be a prokaryotic cell, suchas a bacterial cell. A host strain may be chosen which modulates theexpression of the inserted gene sequences, or modifies and processes thegene product in the specific fashion desired. Expression from certainpromoters can be elevated in the presence of certain inducers; thusexpression of the genetically engineered polypeptide may be controlled.Furthermore, different host cells have characteristics and specificmechanisms for the translational and post-translational processing andmodification (e.g., phosphorylation, cleavage) of proteins. Appropriatecell lines can be chosen to ensure the desired modifications andprocessing of the foreign protein expressed.

Introduction of the nucleic acids and nucleic acid constructs of theinvention into the host cell can be effected by calcium phosphatetransfection, DEAE-dextran mediated transfection, cationiclipid-mediated transfection, electroporation, transduction, infection,or other methods. Such methods are described in many standard laboratorymanuals, such as Davis et al., Basic Methods In Molecular Biology(1986). It is specifically contemplated that the polypeptides of thepresent invention may in fact be expressed by a host cell lacking arecombinant vector.

In addition to encompassing host cells containing the vector constructsdiscussed herein, the invention also encompasses primary, secondary, andimmortalized host cells of vertebrate origin, particularly mammalianorigin, that have been engineered to delete or replace endogenousgenetic material (e.g., the coding sequence corresponding to aTherapeutic protein may be replaced with an albumin fusion proteincorresponding to the Therapeutic protein), and/or to include geneticmaterial (e.g., heterologous polynucleotide sequences such as forexample, an albumin fusion protein of the invention corresponding to theTherapeutic protein may be included). The genetic material operablyassociated with the endogenous polynucleotide may activate, alter,and/or amplify endogenous polynucleotides.

In addition, techniques known in the art may be used to operablyassociate heterologous polynucleotides (e.g., polynucleotides encodingan albumin protein, or a fragment or variant thereof) and/orheterologous control regions (e.g., promoter and/or enhancer) withendogenous polynucleotide sequences encoding a Therapeutic protein viahomologous recombination (see, e.g., U.S. Pat. No. 5,641,670, issuedJun. 24, 1997; International Publication Number WO 96/29411;International Publication Number WO 94/12650; Koller et al., Proc. Natl.Acad. Sci. USA 86:8932-8935 (1989); and Zijlstra et al., Nature342:435-438 (1989), the disclosures of each of which are incorporated byreference in their entireties).

Albumin fusion proteins of the invention can be recovered and purifiedfrom recombinant cell cultures by well-known methods including ammoniumsulfate or ethanol precipitation, acid extraction, anion or cationexchange chromatography, phosphocellulose chromatography, hydrophobicinteraction chromatography, affinity chromatography, hydroxylapatitechromatography, hydrophobic charge interaction chromatography and lectinchromatography. Most preferably, high performance liquid chromatography(“HPLC”) is employed for purification.

In preferred embodiments the albumin fusion proteins of the inventionare purified using Anion Exchange Chromatography including, but notlimited to, chromatography on Q-sepharose, DEAE sepharose, poros HQ,poros DEAE, Toyopearl Q, Toyopearl QAE, Toyopearl DEAE, Resource/SourceQ and DEAE, Fractogel Q and DEAE columns.

In specific embodiments the albumin fusion proteins of the invention arepurified using Cation Exchange Chromatography including, but not limitedto, SP-sepharose, CM sepharose, poros HS, poros CM, Toyopearl SP,Toyopearl CM, Resource/Source S and CM, Fractogel S and CM columns andtheir equivalents and comparables.

In specific embodiments the albumin fusion proteins of the invention arepurified using Hydrophobic Interaction Chromatography including, but notlimited to, Phenyl, Butyl, Methyl, Octyl, Hexyl-sepharose, poros Phenyl,Butyl, Methyl, Octyl, Hexyl, Toyopearl Phenyl, Butyl, Methyl, Octyl,Hexyl Resource/Source Phenyl, Butyl, Methyl, Octyl, Hexyl, FractogelPhenyl, Butyl, Methyl, Octyl, Hexyl columns and their equivalents andcomparables.

In specific embodiments the albumin fusion proteins of the invention arepurified using Size Exclusion Chromatography including, but not limitedto, sepharose S100, S200, S300, superdex resin columns and theirequivalents and comparables.

In specific embodiments the albumin fusion proteins of the invention arepurified using Affinity Chromatography including, but not limited to,Mimetic Dye affinity, peptide affinity and antibody affinity columnsthat are selective for either the HSA or the “fusion target” molecules.

In preferred embodiments albumin fusion proteins of the invention arepurified using one or more Chromatography methods listed above. In otherpreferred embodiments, albumin fusion proteins of the invention arepurified using one or more of the following Chromatography columns, Qsepharose FF column, SP Sepharose FF column, Q Sepharose HighPerformance Column, Blue Sepharose FF column, Blue Column, PhenylSepharose FF column, DEAE Sepharose FF, or Methyl Column.

Additionally, albumin fusion proteins of the invention may be purifiedusing the process described in PCT International Publication WO 00/44772which is herein incorporated by reference in its entirety. One of skillin the art could easily modify the process described therein for use inthe purification of albumin fusion proteins of the invention.

Albumin fusion proteins of the present invention may be recovered from:products of chemical synthetic procedures; and products produced byrecombinant techniques from a prokaryotic or eukaryotic host, including,for example, bacterial, yeast, higher plant, insect, and mammaliancells. Depending upon the host employed in a recombinant productionprocedure, the polypeptides of the present invention may be glycosylatedor may be non-glycosylated. In addition, albumin fusion proteins of theinvention may also include an initial modified methionine residue, insome cases as a result of host-mediated processes. Thus, it is wellknown in the art that the N-terminal methionine encoded by thetranslation initiation codon generally is removed with high efficiencyfrom any protein after translation in all eukaryotic cells. While theN-terminal methionine on most proteins also is efficiently removed inmost prokaryotes, for some proteins, this prokaryotic removal process isinefficient, depending on the nature of the amino acid to which theN-terminal methionine is covalently linked.

In one embodiment, the yeast Pichia pastoris is used to express albuminfusion proteins of the invention in a eukaryotic system. Pichia pastorisis a methylotrophic yeast which can metabolize methanol as its solecarbon source. A main step in the methanol metabolization pathway is theoxidation of methanol to formaldehyde using O₂. This reaction iscatalyzed by the enzyme alcohol oxidase. In order to metabolize methanolas its sole carbon source, Pichia pastoris must generate high levels ofalcohol oxidase due, in part, to the relatively low affinity of alcoholoxidase for O₂. Consequently, in a growth medium depending on methanolas a main carbon source, the promoter region of one of the two alcoholoxidase genes (AOX1) is highly active. In the presence of methanol,alcohol oxidase produced from the AOX1 gene comprises up toapproximately 30% of the total soluble protein in Pichia pastoris. SeeEllis, S. B., et al., Mol. Cell. Biol. 5:1111-21 (1985); Koutz, P. J, etal., Yeast 5:167-77 (1989); Tschopp, J. F., et al., Nucl. Acids Res.15:3859-76 (1987). Thus, a heterologous coding sequence, such as, forexample, a polynucleotide of the present invention, under thetranscriptional regulation of all or part of the AOX1 regulatorysequence is expressed at exceptionally high levels in Pichia yeast grownin the presence of methanol.

In one example, the plasmid vector pPIC9K is used to express DNAencoding an albumin fusion protein of the invention, as set forthherein, in a Pichea yeast system essentially as described in “PichiaProtocols: Methods in Molecular Biology,” D. R. Higgins and J. Cregg,eds. The Humana Press, Totowa, N. J., 1998. This expression vectorallows expression and secretion of a polypeptide of the invention byvirtue of the strong AOX1 promoter linked to the Pichia pastorisalkaline phosphatase (PHO) secretory signal peptide (i.e., leader)located upstream of a multiple cloning site.

Many other yeast vectors could be used in place of pPIC9K, such as,pYES2, pYD1, pTEF1/Zeo, pYES2/GS, pPICZ, pGAPZ, pGAPZalpha, pPIC9,pPIC3.5, pHIL-D2, pHIL-S1, pPIC3.5K, and PA0815, as one skilled in theart would readily appreciate, as long as the proposed expressionconstruct provides appropriately located signals for transcription,translation, secretion (if desired), and the like, including an in-frameAUG as required.

In another embodiment, high-level expression of a heterologous codingsequence, such as, for example, a polynucleotide encoding an albuminfusion protein of the present invention, may be achieved by cloning theheterologous polynucleotide of the invention into an expression vectorsuch as, for example, pGAPZ or pGAPZalpha, and growing the yeast culturein the absence of methanol.

In addition, albumin fusion proteins of the invention can be chemicallysynthesized using techniques known in the art (e.g., see Creighton,1983, Proteins: Structures and Molecular Principles, W.H. Freeman & Co.,N.Y., and Hunkapiller et al., Nature, 310:105-111 (1984)). For example,a polypeptide corresponding to a fragment of a polypeptide can besynthesized by use of a peptide synthesizer. Furthermore, if desired,nonclassical amino acids or chemical amino acid analogs can beintroduced as a substitution or addition into the polypeptide sequence.Non-classical amino acids include, but are not limited to, to theD-isomers of the common amino acids, 2,4-diaminobutyric acid, a-aminoisobutyric acid, 4-aminobutyric acid, Abu, 2-amino butyric acid, g-Abu,e-Ahx, 6-amino hexanoic acid, Aib, 2-amino isobutyric acid, 3-aminopropionic acid, ornithine, norleucine, norvaline, hydroxyproline,sarcosine, citrulline, homocitrulline, cysteic acid, t-butylglycine,t-butylalanine, phenylglycine, cyclohexylalanine, b-alanine,fluoro-amino acids, designer amino acids such as b-methyl amino acids,Ca-methyl amino acids, Na-methyl amino acids, and amino acid analogs ingeneral. Furthermore, the amino acid can be D (dextrorotary) or L(levorotary).

The invention encompasses albumin fusion proteins of the presentinvention which are differentially modified during or after translation,e.g., by glycosylation, acetylation, phosphorylation, amidation,derivatization by known protecting/blocking groups, proteolyticcleavage, linkage to an antibody molecule or other cellular ligand, etc.Any of numerous chemical modifications may be carried out by knowntechniques, including but not limited, to specific chemical cleavage bycyanogen bromide, trypsin, chymotrypsin, papain, V8 protease, NaBH₄;acetylation, formylation, oxidation, reduction; metabolic synthesis inthe presence of tunicamycin; etc.

Additional post-translational modifications encompassed by the inventioninclude, for example, e.g., N-linked or O-linked carbohydrate chains,processing of N-terminal or C-terminal ends), attachment of chemicalmoieties to the amino acid backbone, chemical modifications of N-linkedor O-linked carbohydrate chains, and addition or deletion of anN-terminal methionine residue as a result of procaryotic host cellexpression. The albumin fusion proteins may also be modified with adetectable label, such as an enzymatic, fluorescent, isotopic oraffinity label to allow for detection and isolation of the protein.

Examples of suitable enzymes include horseradish peroxidase, alkalinephosphatase, beta-galactosidase, or acetylcholinesterase; examples ofsuitable prosthetic group complexes include streptavidin/biotin andavidin/biotin; examples of suitable fluorescent materials includeumbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine,dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; anexample of a luminescent material includes luminol; examples ofbioluminescent materials include luciferase, luciferin, and aequorin;and examples of suitable radioactive material include iodine (¹²¹I ¹²³I,¹²⁵I, ¹³¹I), carbon (¹⁴C) sulfur (³⁵S), tritium (³H), indium (¹¹¹In,¹¹²In, ^(113m)In, ^(115m)In), technetium (⁹⁹Tc, ^(99m)Tc), thallium(²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga), palladium (¹⁰³Pd), molybdenum (⁹⁹Mo),xenon (¹³³Xe), fluorine (¹⁸F), ¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰La, ¹⁷⁵Yb,¹⁶⁶Ho, ⁹⁰Y, ⁴⁷Se, ¹⁸⁶Re, ¹⁸⁸Re, ¹⁴²Pr, ¹⁰⁵Rh, and ⁹⁷Ru.

In specific embodiments, albumin fusion proteins of the presentinvention or fragments or variants thereof are attached to macrocyclicchelators that associate with radiometal ions, including but not limitedto, ¹⁷⁷Lu, ⁹⁰Y, ¹⁶⁶Ho, and ¹⁵³Sm, to polypeptides. In a preferredembodiment, the radiometal ion associated with the macrocyclic chelatorsis ¹¹¹In. In another preferred embodiment, the radiometal ion associatedwith the macrocyclic chelator is ⁹⁰Y. In specific embodiments, themacrocyclic chelator is1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetic acid (DOTA). Inother specific embodiments, DOTA is attached to an antibody of theinvention or fragment thereof via linker molecule. Examples of linkermolecules useful for conjugating DOTA to a polypeptide are commonlyknown in the art—see, for example, DeNardo et al., Clin Cancer Res.4(10):2483-90 (1998); Peterson et al., Bioconjug. Chem. 10(4):553-7(1999); and Zimmerman et al, Nucl. Med. Biol. 26(8):943-50 (1999); whichare hereby incorporated by reference in their entirety.

As mentioned, the albumin fusion proteins of the invention may bemodified by either natural processes, such as post-translationalprocessing, or by chemical modification techniques which are well knownin the art. It will be appreciated that the same type of modificationmay be present in the same or varying degrees at several sites in agiven polypeptide. Polypeptides of the invention may be branched, forexample, as a result of ubiquitination, and they may be cyclic, with orwithout branching. Cyclic, branched, and branched cyclic polypeptidesmay result from posttranslation natural processes or may be made bysynthetic methods. Modifications include acetylation, acylation,ADP-ribosylation, amidation, covalent attachment of flavin, covalentattachment of a heme moiety, covalent attachment of a nucleotide ornucleotide derivative, covalent attachment of a lipid or lipidderivative, covalent attachment of phosphotidylinositol, cross-linking,cyclization, disulfide bond formation, demethylation, formation ofcovalent cross-links, formation of cysteine, formation of pyroglutamate,formylation, gamma-carboxylation, glycosylation, GPI anchor formation,hydroxylation, iodination, methylation, myristylation, oxidation,pegylation, proteolytic processing, phosphorylation, prenylation,racemization, selenoylation, sulfation, transfer-RNA mediated additionof amino acids to proteins such as arginylation, and ubiquitination.(See, for instance, PROTEINS—STRUCTURE AND MOLECULAR PROPERTIES, 2ndEd., T. E. Creighton, W. H. Freeman and Company, New York (1993);POST-TRANSLATIONAL COVALENT MODIFICATION OF PROTEINS, B. C. Johnson,Ed., Academic Press, New York, pgs. 1-12 (1983); Seifter et al., Meth.Enzymol. 182:626-646 (1990); Rattan et al., Ann. N.Y. Acad. Sci.663:48-62 (1992)).

Albumin fusion proteins of the invention and antibodies that bind aTherapeutic protein or fragments or variants thereof can be fused tomarker sequences, such as a peptide to facilitate purification. Inpreferred embodiments, the marker amino acid sequence is ahexa-histidine peptide, such as the tag provided in a pQE vector(QIAGEN, Inc., 9259 Eton Avenue, Chatsworth, Calif., 91311), amongothers, many of which are commercially available. As described in Gentzet al., Proc. Natl. Acad. Sci. USA 86:821-824 (1989), for instance,hexa-histidine provides for convenient purification of the fusionprotein. Other peptide tags useful for purification include, but are notlimited to, the “HA” tag, which corresponds to an epitope derived fromthe influenza hemagglutinin protein (Wilson et al., Cell 37:767 (1984))and the “flag” tag.

Further, an albumin fusion protein of the invention may be conjugated toa therapeutic moiety such as a cytotoxin, e.g., a cytostatic orcytocidal agent, a therapeutic agent or a radioactive metal ion, e.g.,alpha-emitters such as, for example, 213Bi. A cytotoxin or cytotoxicagent includes any agent that is detrimental to cells. Examples includepaclitaxol, cytochalasin B, gramicidin D, ethidium bromide, emetine,mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicin,doxorubicin, daunorubicin, dihydroxy anthracin dione, mitoxantrone,mithramycin, actinomycin D, 1-dehydrotestosterone, glucocorticoids,procaine, tetracaine, lidocaine, propranolol, and puromycin and analogsor homologs thereof. Therapeutic agents include, but are not limited to,antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine,cytarabine, 5-fluorouracil decarbazine), alkylating agents (e.g.,mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BSNU) andlomustine (CCNU), cyclothosphamide, busulfan, dibromomannitol,streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP)cisplatin), anthracyclines (e.g., daunorubicin (formerly daunomycin) anddoxorubicin), antibiotics (e.g., dactinomycin (formerly actinomycin),bleomycin, mithramycin, and anthramycin (AMC)), and anti-mitotic agents(e.g., vincristine and vinblastine).

The conjugates of the invention can be used for modifying a givenbiological response, the therapeutic agent or drug moiety is not to beconstrued as limited to classical chemical therapeutic agents. Forexample, the drug moiety may be a protein or polypeptide possessing adesired biological activity. Such proteins may include, for example, atoxin such as abrin, ricin A, pseudomonas exotoxin, or diphtheria toxin;a protein such as tumor necrosis factor, alpha-interferon, β-interferon,nerve growth factor, platelet derived growth factor, tissue plasminogenactivator, an apoptotic agent, e.g., TNF-alpha, TNF-beta, AIM I (See,International Publication No. WO 97/33899), AIM II (See, InternationalPublication No. WO 97/34911), Fas Ligand (Takahashi et al., Int.Immunol., 6:1567-1574 (1994)), VEGI (See, International Publication No.WO 99/23105), a thrombotic agent or an anti-angiogenic agent, e.g.,angiostatin or endostatin; or, biological response modifiers such as,for example, lymphokines, interleukin-1 (“IL-1”), interleukin-2(“IL-2”), interleukin-6 (“IL-6”), granulocyte macrophage colonystimulating factor (“GM-CSF”), granulocyte colony stimulating factor(“G-CSF”), or other growth factors. Techniques for conjugating suchtherapeutic moiety to proteins (e.g., albumin fusion proteins) are wellknown in the art.

Albumin fusion proteins may also be attached to solid supports, whichare particularly useful for immunoassays or purification of polypeptidesthat are bound by, that bind to, or associate with albumin fusionproteins of the invention. Such solid supports include, but are notlimited to, glass, cellulose, polyacrylamide, nylon, polystyrene,polyvinyl chloride or polypropylene.

Albumin fusion proteins, with or without a therapeutic moiety conjugatedto it, administered alone or in combination with cytotoxic factor(s)and/or cytokine(s) can be used as a therapeutic.

In embodiments where the albumin fusion protein of the inventioncomprises only the VH domain of an antibody that binds a Therapeuticprotein, it may be necessary and/or desirable to coexpress the fusionprotein with the VL domain of the same antibody that binds a Therapeuticprotein, such that the VH-albumin fusion protein and VL protein willassociate (either covalently or non-covalently) post-translationally.

In embodiments where the albumin fusion protein of the inventioncomprises only the VL domain of an antibody that binds a Therapeuticprotein, it may be necessary and/or desirable to coexpress the fusionprotein with the VH domain of the same antibody that binds a Therapeuticprotein, such that the VL-albumin fusion protein and VH protein willassociate (either covalently or non-covalently) post-translationally.

Some Therapeutic antibodies are bispecific antibodies, meaning theantibody that binds a Therapeutic protein is an artificial hybridantibody having two different heavy/light chain pairs and two differentbinding sites. In order to create an albumin fusion proteincorresponding to that Therapeutic protein, it is possible to create analbumin fusion protein which has an scFv fragment fused to both the N-and C-terminus of the albumin protein moiety. More particularly, thescFv fused to the N-terminus of albumin would correspond to one of theheavy/light (VH/VL) pairs of the original antibody that binds aTherapeutic protein and the scFv fused to the C-terminus of albuminwould correspond to the other heavy/light (VH/VL) pair of the originalantibody that binds a Therapeutic protein.

Also provided by the invention are chemically modified derivatives ofthe albumin fusion proteins of the invention which may provideadditional advantages such as increased solubility, stability andcirculating time of the polypeptide, or decreased immunogenicity (seeU.S. Pat. No. 4,179,337). The chemical moieties for derivitization maybe selected from water soluble polymers such as polyethylene glycol,ethylene glycol/propylene glycol copolymers, carboxymethylcellulose,dextran, polyvinyl alcohol and the like. The albumin fusion proteins maybe modified at random positions within the molecule, or at predeterminedpositions within the molecule and may include one, two, three or moreattached chemical moieties.

The polymer may be of any molecular weight, and may be branched orunbranched. For polyethylene glycol, the preferred molecular weight isbetween about 1 kDa and about 100 kDa (the term “about” indicating thatin preparations of polyethylene glycol, some molecules will weigh more,some less, than the stated molecular weight) for ease in handling andmanufacturing. Other sizes may be used, depending on the desiredtherapeutic profile (e.g., the duration of sustained release desired,the effects, if any on biological activity, the ease in handling, thedegree or lack of antigenicity and other known effects of thepolyethylene glycol to a Therapeutic protein or analog). For example,the polyethylene glycol may have an average molecular weight of about200, 500, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 5500,6000, 6500, 7000, 7500, 8000, 8500, 9000, 9500, 10,000, 10,500, 11,000,11,500, 12,000, 12,500, 13,000, 13,500, 14,000, 14,500, 15,000, 15,500,16,000, 16,500, 17,000, 17,500, 18,000, 18,500, 19,000, 19,500, 20,000,25,000, 30,000, 35,000, 40,000, 45,000, 50,000, 55,000, 60,000, 65,000,70,000, 75,000, 80,000, 85,000, 90,000, 95,000, or 100,000 kDa.

As noted above, the polyethylene glycol may have a branched structure.Branched polyethylene glycols are described, for example, in U.S. Pat.No. 5,643,575; Morpurgo et al., Appl. Biochem. Biotechnol. 56:59-72(1996); Vorobjev et al., Nucleosides Nucleotides 18:2745-2750 (1999);and Caliceti et al., Bioconjug. Chem. 10:638-646 (1999), the disclosuresof each of which are incorporated herein by reference.

The polyethylene glycol molecules (or other chemical moieties) should beattached to the protein with consideration of effects on functional orantigenic domains of the protein. There are a number of attachmentmethods available to those skilled in the art, such as, for example, themethod disclosed in EP 0 401 384 (coupling PEG to G-CSF), hereinincorporated by reference; see also Malik et al., Exp. Hematol.20:1028-1035 (1992), reporting pegylation of GM-CSF using tresylchloride. For example, polyethylene glycol may be covalently boundthrough amino acid residues via reactive group, such as a free amino orcarboxyl group. Reactive groups are those to which an activatedpolyethylene glycol molecule may be bound. The amino acid residueshaving a free amino group may include lysine residues and the N-terminalamino acid residues; those having a free carboxyl group may includeaspartic acid residues glutamic acid residues and the C-terminal aminoacid residue. Sulfhydryl groups may also be used as a reactive group forattaching the polyethylene glycol molecules. Preferred for therapeuticpurposes is attachment at an amino group, such as attachment at theN-terminus or lysine group.

As suggested above, polyethylene glycol may be attached to proteins vialinkage to any of a number of amino acid residues. For example,polyethylene glycol can be linked to proteins via covalent bonds tolysine, histidine, aspartic acid, glutamic acid, or cysteine residues.One or more reaction chemistries may be employed to attach polyethyleneglycol to specific amino acid residues (e.g., lysine, histidine,aspartic acid, glutamic acid, or cysteine) of the protein or to morethan one type of amino acid residue (e.g., lysine, histidine, asparticacid, glutamic acid, cysteine and combinations thereof) of the protein.

One may specifically desire proteins chemically modified at theN-terminus. Using polyethylene glycol as an illustration of the presentcomposition, one may select from a variety of polyethylene glycolmolecules (by molecular weight, branching, etc.), the proportion ofpolyethylene glycol molecules to protein (polypeptide) molecules in thereaction mix, the type of pegylation reaction to be performed, and themethod of obtaining the selected N-terminally pegylated protein. Themethod of obtaining the N-terminally pegylated preparation (i.e.,separating this moiety from other monopegylated moieties if necessary)may be by purification of the N-terminally pegylated material from apopulation of pegylated protein molecules. Selective proteins chemicallymodified at the N-terminus modification may be accomplished by reductivealkylation which exploits differential reactivity of different types ofprimary amino groups (lysine versus the N-terminal) available forderivatization in a particular protein. Under the appropriate reactionconditions, substantially selective derivatization of the protein at theN-terminus with a carbonyl group containing polymer is achieved.

As indicated above, pegylation of the albumin fusion proteins of theinvention may be accomplished by any number of means. For example,polyethylene glycol may be attached to the albumin fusion protein eitherdirectly or by an intervening linker. Linkerless systems for attachingpolyethylene glycol to proteins are described in Delgado et al., Crit.Rev. Thera. Drug Carrier Sys. 9:249-304 (1992); Francis et al., Intern.J. of Hematol. 68:1-18 (1998); U.S. Pat. No. 4,002,531; U.S. Pat. No.5,349,052; WO 95/06058; and WO 98/32466, the disclosures of each ofwhich are incorporated herein by reference.

One system for attaching polyethylene glycol directly to amino acidresidues of proteins without an intervening linker employs tresylatedMPEG, which is produced by the modification of monmethoxy polyethyleneglycol (MPEG) using tresylchloride (ClSO₂CH₂CF₃). Upon reaction ofprotein with tresylated MPEG, polyethylene glycol is directly attachedto amine groups of the protein. Thus, the invention includesprotein-polyethylene glycol conjugates produced by reacting proteins ofthe invention with a polyethylene glycol molecule having a2,2,2-trifluoreothane sulphonyl group.

Polyethylene glycol can also be attached to proteins using a number ofdifferent intervening linkers. For example, U.S. Pat. No. 5,612,460, theentire disclosure of which is incorporated herein by reference,discloses urethane linkers for connecting polyethylene glycol toproteins. Protein-polyethylene glycol conjugates wherein thepolyethylene glycol is attached to the protein by a linker can also beproduced by reaction of proteins with compounds such asMPEG-succinimidylsuccinate, MPEG activated with1,1′-carbonyldiimidazole, MPEG-2,4,5-trichloropenylcarbonate,MPEG-p-nitrophenolcarbonate, and various MPEG-succinate derivatives. Anumber of additional polyethylene glycol derivatives and reactionchemistries for attaching polyethylene glycol to proteins are describedin International Publication No. WO 98/32466, the entire disclosure ofwhich is incorporated herein by reference. Pegylated protein productsproduced using the reaction chemistries set out herein are includedwithin the scope of the invention.

The number of polyethylene glycol moieties attached to each albuminfusion protein of the invention (i.e., the degree of substitution) mayalso vary. For example, the pegylated proteins of the invention may belinked, on average, to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 15, 17, 20, ormore polyethylene glycol molecules. Similarly, the average degree ofsubstitution within ranges such as 1-3, 2-4, 3-5, 4-6, 5-7, 6-8, 7-9,8-10, 9-11, 10-12, 11-13, 12-14, 13-15, 14-16, 15-17, 16-18, 17-19, or18-20 polyethylene glycol moieties per protein molecule. Methods fordetermining the degree of substitution are discussed, for example, inDelgado et al., Crit. Rev. Thera. Drug Carrier Sys. 9:249-304 (1992).

The polypeptides of the invention can be recovered and purified fromchemical synthesis and recombinant cell cultures by standard methodswhich include, but are not limited to, ammonium sulfate or ethanolprecipitation, acid extraction, anion or cation exchange chromatography,phosphocellulose chromatography, hydrophobic interaction chromatography,affinity chromatography, hydroxylapatite chromatography and lectinchromatography. Most preferably, high performance liquid chromatography(“HPLC”) is employed for purification. Well known techniques forrefolding protein may be employed to regenerate active conformation whenthe polypeptide is denatured during isolation and/or purification.

The presence and quantity of albumin fusion proteins of the inventionmay be determined using ELISA, a well known immunoassay known in theart. In one ELISA protocol that would be useful fordetecting/quantifying albumin fusion proteins of the invention,comprises the steps of coating an ELISA plate with an anti-human serumalbumin antibody, blocking the plate to prevent non-specific binding,washing the ELISA plate, adding a solution containing the albumin fusionprotein of the invention (at one or more different concentrations),adding a secondary anti-Therapeutic protein specific antibody coupled toa detectable label (as described herein or otherwise known in the art),and detecting the presence of the secondary antibody. In an alternateversion of this protocol, the ELISA plate might be coated with theanti-Therapeutic protein specific antibody and the labeled secondaryreagent might be the anti-human albumin specific antibody.

Uses of the Polynucleotides

Each of the polynucleotides identified herein can be used in numerousways as reagents. The following description should be consideredexemplary and utilizes known techniques.

The polynucleotides of the present invention are useful to produce thealbumin fusion proteins of the invention. As described in more detailbelow, polynucleotides of the invention (encoding albumin fusionproteins) may be used in recombinant DNA methods useful in geneticengineering to make cells, cell lines, or tissues that express thealbumin fusion protein encoded by the polynucleotides encoding albuminfusion proteins of the invention.

Polynucleotides of the present invention are also useful in genetherapy. One goal of gene therapy is to insert a normal gene into anorganism having a defective gene, in an effort to correct the geneticdefect. The polynucleotides disclosed in the present invention offer ameans of targeting such genetic defects in a highly accurate manner.Another goal is to insert a new gene that was not present in the hostgenome, thereby producing a new trait in the host cell. Additionalnon-limiting examples of gene therapy methods encompassed by the presentinvention are more thoroughly described elsewhere herein (see, e.g., thesections labeled “Gene Therapy”, and Examples 63 and 64).

Uses of the Polypeptides

Each of the polypeptides identified herein can be used in numerous ways.The following description should be considered exemplary and utilizesknown techniques.

Albumin fusion proteins of the invention are useful to provideimmunological probes for differential identification of the tissue(s)(e.g., immunohistochemistry assays such as, for example, ABCimmunoperoxidase (Hsu et al., J. Histochem. Cytochem. 29:577-580 (1981))or cell type(s) (e.g., immunocytochemistry assays).

Albumin fusion proteins can be used to assay levels of polypeptides in abiological sample using classical immunohistological methods known tothose of skill in the art (e.g., see Jalkanen, et al., J. Cell. Biol.101:976-985 (1985); Jalkanen, et al., J. Cell. Biol. 105:3087-3096(1987)). Other methods useful for detecting protein gene expressioninclude immunoassays, such as the enzyme linked immunosorbent assay(ELISA) and the radioimmunoassay (RIA). Suitable assay labels are knownin the art and include enzyme labels, such as, glucose oxidase;radioisotopes, such as iodine (¹³¹I, ¹²⁵I, ¹²³I, ¹²¹I) carbon (¹⁴C),sulfur (³⁵S), tritium (³H), indium (^(115m)In, ^(113m)In, ¹¹²In, ¹¹¹In),and technetium (⁹⁹Tc, ^(99m)Tc), thallium (²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga),palladium (¹⁰³Pd), molybdenum (⁹⁹Mo), xenon (¹³³Xe), fluorine (¹⁸F),¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰La, ¹⁷⁵Yb, ¹⁶⁶Ho, ⁹⁰Y, ⁴⁷Sc, ¹⁸⁶Re,¹⁸⁸Re, ¹⁴²Pr, ¹⁰⁵Rh, ⁹⁷Ru; luminescent labels, such as luminol; andfluorescent labels, such as fluorescein and rhodamine, and biotin.

Albumin fusion proteins of the invention can also be detected in vivo byimaging. Labels or markers for in vivo imaging of protein include thosedetectable by X-radiography, nuclear magnetic resonance (NMR) orelectron spin relaxation (ESR). For X-radiography, suitable labelsinclude radioisotopes such as barium or cesium, which emit detectableradiation but are not overtly harmful to the subject. Suitable markersfor NMR and ESR include those with a detectable characteristic spin,such as deuterium, which may be incorporated into the albumin fusionprotein by labeling of nutrients given to a cell line expressing thealbumin fusion protein of the invention.

An albumin fusion protein which has been labeled with an appropriatedetectable imaging moiety, such as a radioisotope (for example, ¹³¹I,¹¹²In, ^(99m)Tc, (¹³¹I, ¹²⁵I, ¹²³I, ¹²¹I), carbon (¹⁴C), sulfur (³⁵S),tritium (³H), H), indium (^(115m)In, ^(113m)In, ¹¹²In, ¹¹¹In), andtechnetium (⁹⁹Tc, ^(99m)Tc), thallium (²⁰¹Ti), gallium (⁶⁸Ga, ⁶⁷Ga),palladium (¹⁰³Pd), molybdenum (⁹⁹Mo), xenon (¹³³Xe), fluorine (¹⁸F,¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁴⁹Pm, ¹⁴⁰La, ¹⁷⁵Yb, ¹⁶⁶Ho, ⁹⁰Y, ⁴⁷Sc, ¹⁸⁶Re,¹⁸⁸Re, ¹⁴²Pr, ¹⁰⁵Rh, ⁹⁷Ru), a radio-opaque substance, or a materialdetectable by nuclear magnetic resonance, is introduced (for example,parenterally, subcutaneously or intraperitoneally) into the mammal to beexamined for immune system disorder. It will be understood in the artthat the size of the subject and the imaging system used will determinethe quantity of imaging moiety needed to produce diagnostic images. Inthe case of a radioisotope moiety, for a human subject, the quantity ofradioactivity injected will normally range from about 5 to 20millicuries of ^(99m)Tc. The labeled albumin fusion protein will thenpreferentially accumulate at locations in the body (e.g., organs, cells,extracellular spaces or matrices) where one or more receptors, ligandsor substrates (corresponding to that of the Therapeutic protein used tomake the albumin fusion protein of the invention) are located.Alternatively, in the case where the albumin fusion protein comprises atleast a fragment or variant of a Therapeutic antibody, the labeledalbumin fusion protein will then preferentially accumulate at thelocations in the body (e.g., organs, cells, extracellular spaces ormatrices) where the polypeptides/epitopes corresponding to those boundby the Therapeutic antibody (used to make the albumin fusion protein ofthe invention) are located. In vivo tumor imaging is described in S. W.Burchiel et al., “Immunopharmacokinetics of Radiolabeled Antibodies andTheir Fragments” (Chapter 13 in Tumor Imaging: The RadiochemicalDetection of Cancer, S. W. Burchiel and B. A. Rhodes, eds., MassonPublishing Inc. (1982)). The protocols described therein could easily bemodified by one of skill in the art for use with the albumin fusionproteins of the invention.

In one embodiment, the invention provides a method for the specificdelivery of albumin fusion proteins of the invention to cells byadministering albumin fusion proteins of the invention (e.g.,polypeptides encoded by polynucleotides encoding albumin fusion proteinsof the invention and/or antibodies) that are associated withheterologous polypeptides or nucleic acids. In one example, theinvention provides a method for delivering a Therapeutic protein intothe targeted cell. In another example, the invention provides a methodfor delivering a single stranded nucleic acid (e.g., antisense orribozymes) or double stranded nucleic acid (e.g., DNA that can integrateinto the cell's genome or replicate episomally and that can betranscribed) into the targeted cell.

In another embodiment, the invention provides a method for the specificdestruction of cells (e.g., the destruction of tumor cells) byadministering albumin fusion proteins of the invention in associationwith toxins or cytotoxic prodrugs.

By “toxin” is meant one or more compounds that bind and activateendogenous cytotoxic effector systems, radioisotopes, holotoxins,modified toxins, catalytic subunits of toxins, or any molecules orenzymes not normally present in or on the surface of a cell that underdefined conditions cause the cell's death. Toxins that may be usedaccording to the methods of the invention include, but are not limitedto, radioisotopes known in the art, compounds such as, for example,antibodies (or complement fixing containing portions thereof) that bindan inherent or induced endogenous cytotoxic effector system, thymidinekinase, endonuclease, RNAse, alpha toxin, ricin, abrin, Pseudomonasexotoxin A, diphtheria toxin, saporin, momordin, gelonin, pokeweedantiviral protein, alpha-sarcin and cholera toxin. “Toxin” also includesa cytostatic or cytocidal agent, a therapeutic agent or a radioactivemetal ion, e.g., alpha-emitters such as, for example, ²¹³Bi, or otherradioisotopes such as, for example, ¹⁰³Pd, ¹³³xe, ¹³¹I, ⁶⁸Ge, ⁵⁷Co,⁶⁵Zn, ⁸⁵Sr, ³²P ³⁵S ⁹⁰Y ¹⁵³Sm, ¹⁵³Gd, ¹⁶⁹Yb, ⁵¹Cr, ⁵⁴Mn, ⁷⁵Se, ¹¹³Sn,⁹⁰Yttrium, ¹¹⁷Tin, ¹⁸⁶Rhenium, ¹⁶⁶Holmium, and ¹⁸⁸Rhenium; luminescentlabels, such as luminol; and fluorescent labels, such as fluorescein andrhodamine, and biotin. In a specific embodiment, the invention providesa method for the specific destruction of cells (e.g., the destruction oftumor cells) by administering polypeptides of the invention orantibodies of the invention in association with the radioisotope ⁹⁰Y. Inanother specific embodiment, the invention provides a method for thespecific destruction of cells (e.g., the destruction of tumor cells) byadministering polypeptides of the invention or antibodies of theinvention in association with the radioisotope ¹¹¹In. In a furtherspecific embodiment, the invention provides a method for the specificdestruction of cells (e.g., the destruction of tumor cells) byadministering polypeptides of the invention or antibodies of theinvention in association with the radioisotope ¹³¹I.

Techniques known in the art may be applied to label polypeptides of theinvention. Such techniques include, but are not limited to, the use ofbifunctional conjugating agents (see e.g., U.S. Pat. Nos. 5,756,065;5,714,631; 5,696,239; 5,652,361; 5,505,931; 5,489,425; 5,435,990;5,428,139; 5,342,604; 5,274,119; 4,994,560; and 5,808,003; the contentsof each of which are hereby incorporated by reference in its entirety).

The albumin fusion proteins of the present invention are useful fordiagnosis, treatment, prevention and/or prognosis of various disordersin mammals, preferably humans. Such disorders include, but are notlimited to, those described herein under the section heading “BiologicalActivities,” below.

Thus, the invention provides a diagnostic method of a disorder, whichinvolves (a) assaying the expression level of a certain polypeptide incells or body fluid of an individual using an albumin fusion protein ofthe invention; and (b) comparing the assayed polypeptide expressionlevel with a standard polypeptide expression level, whereby an increaseor decrease in the assayed polypeptide expression level compared to thestandard expression level is indicative of a disorder. With respect tocancer, the presence of a relatively high amount of transcript inbiopsied tissue from an individual may indicate a predisposition for thedevelopment of the disease, or may provide a means for detecting thedisease prior to the appearance of actual clinical symptoms. A moredefinitive diagnosis of this type may allow health professionals toemploy preventative measures or aggressive treatment earlier therebypreventing the development or further progression of the cancer.

Moreover, albumin fusion proteins of the present invention can be usedto treat or prevent diseases or conditions such as, for example, neuraldisorders, immune system disorders, muscular disorders, reproductivedisorders, gastrointestinal disorders, pulmonary disorders,cardiovascular disorders, renal disorders, proliferative disorders,and/or cancerous diseases and conditions. For example, patients can beadministered a polypeptide of the present invention in an effort toreplace absent or decreased levels of the polypeptide (e.g., insulin),to supplement absent or decreased levels of a different polypeptide(e.g., hemoglobin S for hemoglobin B, SOD, catalase, DNA repairproteins), to inhibit the activity of a polypeptide (e.g., an oncogeneor tumor suppressor), to activate the activity of a polypeptide (e.g.,by binding to a receptor), to reduce the activity of a membrane boundreceptor by competing with it for free ligand (e.g., soluble TNFreceptors used in reducing inflammation), or to bring about a desiredresponse (e.g., blood vessel growth inhibition, enhancement of theimmune response to proliferative cells or tissues).

In particular, albumin fusion proteins comprising of at least a fragmentor variant of a Therapeutic antibody can also be used to treat disease(as described supra, and elsewhere herein). For example, administrationof an albumin fusion protein comprising of at least a fragment orvariant of a Therapeutic antibody can bind, and/or neutralize thepolypeptide to which the Therapeutic antibody used to make the albuminfusion protein specifically binds, and/or reduce overproduction of thepolypeptide to which the Therapeutic antibody used to make the albuminfusion protein specifically binds. Similarly, administration of analbumin fusion protein comprising of at least a fragment or variant of aTherapeutic antibody can activate the polypeptide to which theTherapeutic antibody used to make the albumin fusion proteinspecifically binds, by binding to the polypeptide bound to a membrane(receptor).

At the very least, the albumin fusion proteins of the invention of thepresent invention can be used as molecular weight markers on SDS-PAGEgels or on molecular sieve gel filtration columns using methods wellknown to those of skill in the art. Albumin fusion proteins of theinvention can also be used to raise antibodies, which in turn may beused to measure protein expression of the Therapeutic protein, albuminprotein, and/or the albumin fusion protein of the invention from arecombinant cell, as a way of assessing transformation of the host cell,or in a biological sample. Moreover, the albumin fusion proteins of thepresent invention can be used to test the biological activitiesdescribed herein.

Diagnostic Assays

The compounds of the present invention are useful for diagnosis,treatment, prevention and/or prognosis of various disorders in mammals,preferably humans. Such disorders include, but are not limited to, thosedescribed for each Therapeutic protein in the corresponding row of Table1 and herein under the section headings “Immune Activity,” “BloodRelated Disorders,” “Hyperproliferative Disorders,” “Renal Disorders,”“Cardiovascular Disorders,” “Respiratory Disorders,” “Anti-AngiogenesisActivity,” “Diseases at the Cellular Level,” “Wound Healing andEpithelial Cell Proliferation,” “Neural Activity and NeurologicalDiseases,” “Endocrine Disorders,” “Reproductive System Disorders,”“Infectious Disease,” “Regeneration,” and/or “GastrointestinalDisorders,” infra.

For a number of disorders, substantially altered (increased ordecreased) levels of gene expression can be detected in tissues, cellsor bodily fluids (e.g., sera, plasma, urine, semen, synovial fluid orspinal fluid) taken from an individual having such a disorder, relativeto a “standard” gene expression level, that is, the expression level intissues or bodily fluids from an individual not having the disorder.Thus, the invention provides a diagnostic method useful during diagnosisof a disorder, which involves measuring the expression level of the geneencoding a polypeptide in tissues, cells or body fluid from anindividual and comparing the measured gene expression level with astandard gene expression level, whereby an increase or decrease in thegene expression level(s) compared to the standard is indicative of adisorder. These diagnostic assays may be performed in vivo or in vitro,such as, for example, on blood samples, biopsy tissue or autopsy tissue.

The present invention is also useful as a prognostic indicator, wherebypatients exhibiting enhanced or depressed gene expression willexperience a worse clinical outcome

By “assaying the expression level of the gene encoding a polypeptide” isintended qualitatively or quantitatively measuring or estimating thelevel of a particular polypeptide (e.g. a polypeptide corresponding to aTherapeutic protein disclosed in Table 1) or the level of the mRNAencoding the polypeptide of the invention in a first biological sampleeither directly (e.g., by determining or estimating absolute proteinlevel or mRNA level) or relatively (e.g., by comparing to thepolypeptide level or mRNA level in a second biological sample).Preferably, the polypeptide expression level or mRNA level in the firstbiological sample is measured or estimated and compared to a standardpolypeptide level or mRNA level, the standard being taken from a secondbiological sample obtained from an individual not having the disorder orbeing determined by averaging levels from a population of individualsnot having the disorder. As will be appreciated in the art, once astandard polypeptide level or mRNA level is known, it can be usedrepeatedly as a standard for comparison.

By “biological sample” is intended any biological sample obtained froman individual, cell line, tissue culture, or other source containingpolypeptides of the invention (including portions thereof) or mRNA. Asindicated, biological samples include body fluids (such as sera, plasma,urine, synovial fluid and spinal fluid) and tissue sources found toexpress the full length or fragments thereof of a polypeptide or mRNA.Methods for obtaining tissue biopsies and body fluids from mammals arewell known in the art. Where the biological sample is to include mRNA, atissue biopsy is the preferred source.

Total cellular RNA can be isolated from a biological sample using anysuitable technique such as the single-stepguanidinium-thiocyanate-phenol-chloroform method described inChomczynski and Sacchi, Anal. Biochem. 162:156-159 (1987). Levels ofmRNA encoding the polypeptides of the invention are then assayed usingany appropriate method. These include Northern blot analysis, S1nuclease mapping, the polymerase chain reaction (PCR), reversetranscription in combination with the polymerase chain reaction(RT-PCR), and reverse transcription in combination with the ligase chainreaction (RT-LCR).

The present invention also relates to diagnostic assays such asquantitative and diagnostic assays for detecting levels of polypeptidesthat bind to, are bound by, or associate with albumin fusion proteins ofthe invention, in a biological sample (e.g., cells and tissues),including determination of normal and abnormal levels of polypeptides.Thus, for instance, a diagnostic assay in accordance with the inventionfor detecting abnormal expression of polypeptides that bind to, arebound by, or associate with albumin fusion proteins compared to normalcontrol tissue samples may be used to detect the presence of tumors.Assay techniques that can be used to determine levels of a polypeptidethat bind to, are bound by, or associate with albumin fusion proteins ofthe present invention in a sample derived from a host are well-known tothose of skill in the art. Such assay methods include radioimmunoassays,competitive-binding assays, Western Blot analysis and ELISA assays.Assaying polypeptide levels in a biological sample can occur using anyart-known method.

Assaying polypeptide levels in a biological sample can occur using avariety of techniques. For example, polypeptide expression in tissuescan be studied with classical immunohistological methods (Jalkanen etal., J. Cell. Biol. 101:976-985 (1985); Jalkanen, M., et al., J. Cell.Biol. 105:3087-3096 (1987)). Other methods useful for detectingpolypeptide gene expression include immunoassays, such as the enzymelinked immunosorbent assay (ELISA) and the radioimmunoassay (MA).Suitable antibody assay labels are known in the art and include enzymelabels, such as, glucose oxidase, and radioisotopes, such as iodine(¹²⁵I, ¹²¹I), carbon (¹⁴C), sulfur (³⁵S), tritium (³H), indium (¹¹²In),and technetium (^(99m)Tc), and fluorescent labels, such as fluoresceinand rhodamine, and biotin.

The tissue or cell type to be analyzed will generally include thosewhich are known, or suspected, to express the gene of interest (such as,for example, cancer). The protein isolation methods employed herein may,for example, be such as those described in Harlow and Lane (Harlow, E.and Lane, D., 1988, “Antibodies: A Laboratory Manual”, Cold SpringHarbor Laboratory Press, Cold Spring Harbor, N.Y.), which isincorporated herein by reference in its entirety. The isolated cells canbe derived from cell culture or from a patient. The analysis of cellstaken from culture may be a necessary step in the assessment of cellsthat could be used as part of a cell-based gene therapy technique or,alternatively, to test the effect of compounds on the expression of thegene.

For example, albumin fusion proteins may be used to quantitatively orqualitatively detect the presence of polypeptides that bind to, arebound by, or associate with albumin fusion proteins of the presentinvention. This can be accomplished, for example, by immunofluorescencetechniques employing a fluorescently labeled albumin fusion proteincoupled with light microscopic, flow cytometric, or fluorimetricdetection.

In a preferred embodiment, albumin fusion proteins comprising at least afragment or variant of an antibody that specifically binds at least aTherapeutic protein disclosed herein (e.g., the Therapeutic proteinsdisclosed in Table 1) or otherwise known in the art may be used toquantitatively or qualitatively detect the presence of gene products orconserved variants or peptide fragments thereof. This can beaccomplished, for example, by immunofluorescence techniques employing afluorescently labeled antibody coupled with light microscopic, flowcytometric, or fluorimetric detection.

The albumin fusion proteins of the present invention may, additionally,be employed histologically, as in immunofluorescence, immunoelectronmicroscopy or non-immunological assays, for in situ detection ofpolypeptides that bind to, are bound by, or associate with an albuminfusion protein of the present invention. In situ detection may beaccomplished by removing a histological specimen from a patient, andapplying thereto a labeled antibody or polypeptide of the presentinvention. The albumin fusion proteins are preferably applied byoverlaying the labeled albumin fusion proteins onto a biological sample.Through the use of such a procedure, it is possible to determine notonly the presence of the polypeptides that bind to, are bound by, orassociate with albumin fusion proteins, but also its distribution in theexamined tissue. Using the present invention, those of ordinary skillwill readily perceive that any of a wide variety of histological methods(such as staining procedures) can be modified in order to achieve suchin situ detection.

Immunoassays and non-immunoassays that detect polypeptides that bind to,are bound by, or associate with albumin fusion proteins will typicallycomprise incubating a sample, such as a biological fluid, a tissueextract, freshly harvested cells, or lysates of cells which have beenincubated in cell culture, in the presence of a detectably labeledantibody capable of binding gene products or conserved variants orpeptide fragments thereof, and detecting the bound antibody by any of anumber of techniques well-known in the art.

The biological sample may be brought in contact with and immobilizedonto a solid phase support or carrier such as nitrocellulose, or othersolid support which is capable of immobilizing cells, cell particles orsoluble proteins. The support may then be washed with suitable buffersfollowed by treatment with the detectably labeled albumin fusion proteinof the invention. The solid phase support may then be washed with thebuffer a second time to remove unbound antibody or polypeptide.Optionally the antibody is subsequently labeled. The amount of boundlabel on solid support may then be detected by conventional means.

By “solid phase support or carrier” is intended any support capable ofbinding a polypeptide (e.g., an albumin fusion protein, or polypeptidethat binds, is bound by, or associates with an albumin fusion protein ofthe invention.) Well-known supports or carriers include glass,polystyrene, polypropylene, polyethylene, dextran, nylon, amylases,natural and modified celluloses, polyacrylamides, gabbros, andmagnetite. The nature of the carrier can be either soluble to someextent or insoluble for the purposes of the present invention. Thesupport material may have virtually any possible structuralconfiguration so long as the coupled molecule is capable of binding to apolypeptide. Thus, the support configuration may be spherical, as in abead, or cylindrical, as in the inside surface of a test tube, or theexternal surface of a rod. Alternatively, the surface may be flat suchas a sheet, test strip, etc. Preferred supports include polystyrenebeads. Those skilled in the art will know many other suitable carriersfor binding antibody or antigen, or will be able to ascertain the sameby use of routine experimentation.

The binding activity of a given lot of albumin fusion protein may bedetermined according to well known methods. Those skilled in the artwill be able to determine operative and optimal assay conditions foreach determination by employing routine experimentation.

In addition to assaying polypeptide levels in a biological sampleobtained from an individual, polypeptide can also be detected in vivo byimaging. For example, in one embodiment of the invention, albumin fusionproteins of the invention are used to image diseased or neoplasticcells.

Labels or markers for in vivo imaging of albumin fusion proteins of theinvention include those detectable by X-radiography, NMR, MRI, CAT-scansor ESR. For X-radiography, suitable labels include radioisotopes such asbarium or cesium, which emit detectable radiation but are not overtlyharmful to the subject. Suitable markers for NMR and ESR include thosewith a detectable characteristic spin, such as deuterium, which may beincorporated into the albumin fusion protein by labeling of nutrients ofa cell line (or bacterial or yeast strain) engineered.

Additionally, albumin fusion proteins of the invention whose presencecan be detected, can be administered. For example, albumin fusionproteins of the invention labeled with a radio-opaque or otherappropriate compound can be administered and visualized in vivo, asdiscussed, above for labeled antibodies. Further, such polypeptides canbe utilized for in vitro diagnostic procedures.

A polypeptide-specific antibody or antibody fragment which has beenlabeled with an appropriate detectable imaging moiety, such as aradioisotope (for example, ¹³¹I, ¹¹²In, ^(99m)Tc), a radio-opaquesubstance, or a material detectable by nuclear magnetic resonance, isintroduced (for example, parenterally, subcutaneously orintraperitoneally) into the mammal to be examined for a disorder. Itwill be understood in the art that the size of the subject and theimaging system used will determine the quantity of imaging moiety neededto produce diagnostic images. In the case of a radioisotope moiety, fora human subject, the quantity of radioactivity injected will normallyrange from about 5 to 20 millicuries of ^(99m)Tc. The labeled albuminfusion protein will then preferentially accumulate at the locations inthe body which contain a polypeptide or other substance that binds to,is bound by or associates with an albumin fusion protein of the presentinvention. In vivo tumor imaging is described in S. W. Burchiel et al.,“Immunopharmacokinetics of Radiolabeled Antibodies and Their Fragments”(Chapter 13 in Tumor Imaging: The Radiochemical Detection of Cancer, S.W. Burchiel and B. A. Rhodes, eds., Masson Publishing Inc. (1982)).

One of the ways in which an albumin fusion protein of the presentinvention can be detectably labeled is by linking the same to a reporterenzyme and using the linked product in an enzyme immunoassay (EIA)(Voller, A., “The Enzyme Linked Immunosorbent Assay (ELISA)”, 1978,Diagnostic Horizons 2:1-7, Microbiological Associates QuarterlyPublication, Walkersville, Md.); Voller et al., J. Clin. Pathol.31:507-520 (1978); Butler, J. E., Meth. Enzymol. 73:482-523 (1981);Maggio, E. (ed.), 1980, Enzyme Immunoassay, CRC Press, Boca Raton,Fla.,; Ishikawa, E. et al., (eds.), 1981, Enzyme Immunoassay, KgakuShoin, Tokyo). The reporter enzyme which is bound to the antibody willreact with an appropriate substrate, preferably a chromogenic substrate,in such a manner as to produce a chemical moiety which can be detected,for example, by spectrophotometric, fluorimetric or by visual means.Reporter enzymes which can be used to detectably label the antibodyinclude, but are not limited to, malate dehydrogenase, staphylococcalnuclease, delta-5-steroid isomerase, yeast alcohol dehydrogenase,alpha-glycerophosphate, dehydrogenase, triose phosphate isomerase,horseradish peroxidase, alkaline phosphatase, asparaginase, glucoseoxidase, beta-galactosidase, ribonuclease, urease, catalase,glucose-6-phosphate dehydrogenase, glucoamylase andacetylcholinesterase. Additionally, the detection can be accomplished bycolorimetric methods which employ a chromogenic substrate for thereporter enzyme. Detection may also be accomplished by visual comparisonof the extent of enzymatic reaction of a substrate in comparison withsimilarly prepared standards.

Albumin fusion proteins may also be radiolabelled and used in any of avariety of other immunoassays. For example, by radioactively labelingthe albumin fusion proteins, it is possible to the use the albuminfusion proteins in a radioimmunoassay (MA) (see, for example, Weintraub,B., Principles of Radioimmunoassays, Seventh Training Course onRadioligand Assay Techniques, The Endocrine Society, March, 1986, whichis incorporated by reference herein). The radioactive isotope can bedetected by means including, but not limited to, a gamma counter, ascintillation counter, or autoradiography.

Additionally, chelator molecules, are known in the art and can be usedto label the Albumin fusion proteins. Chelator molecules may be attachedAlbumin fusion proteins of the invention to facilitate labeling saidprotein with metal ions including radionuclides or fluorescent labels.For example, see Subramanian, R. and Meares, C. F., “BifunctionalChelating Agents for Radiometal-labeled monoclonal Antibodies,” inCancer Imaging with Radiolabeled Antibodies (D. M. Goldenberg, Ed.)Kluwer Academic Publications, Boston; Saji, H., “Targeted delivery ofradiolabeled imaging and therapeutic agents: bifunctionalradiopharmaceuticals.” Crit. Rev. Ther. Drug Carrier Syst. 16:209-244(1999); Srivastava S. C. and Mease R. C., “Progress in research onligands, nuclides and techniques for labeling monoclonal antibodies.”Int. J. Rad. Appl. Instrum. B 18:589-603 (1991); and Liu, S. andEdwards, D. S., “Bifunctional chelators for therapeutic lanthanideradiopharmaceuticals.” Bioconjug. Chem. 12:7-34 (2001). Any chelatorwhich can be covalently bound to said Albumin fusion proteins may beused according to the present invention. The chelator may furthercomprise a linker moiety that connects the chelating moiety to theAlbumin fusion protein.

In one embodiment, the Albumin fusion protein of the invention areattached to an acyclic chelator such as diethylenetriamine-N,N,N′,N″,N″-pentaacetic acid (DPTA), analogues of DPTA, andderivatives of DPTA. As non-limiting examples, the chelator may be2-(p-isothiocyanatobenzyl)-6-methyldiethylenetriaminepentaacetic acid(1B4M-DPTA, also known as MX-DTPA),2-methyl-6-(rho-nitrobenzyl)-1,4,7-triazaheptane-N,N,N′,N″,N″-pentaaceticacid (nitro-1B4M-DTPA or nitro-MX-DTPA);2-(p-isothiocyanatobenzyl)-cyclohexyldiethylenetriaminepentaacetic acid(CHX-DTPA), orN-[2-amino-3-(rho-nitrophenyl)propyl]-trans-cyclohexane-1,2-diamine-N,N′,N″-pentaaceticacid (nitro-CHX-A-DTPA).

In another embodiment, the Albumin fusion protein of the invention areattached to an acyclic terpyridine chelator such as6,6″-bis[[N,N,N″,N″-tetra(carboxymethyl)amino]methyl]-4′-(3-amino-4-methoxyphenyl)-2,2′:6′,2″-terpyridine(TMT-amine).

In specific embodiments, the macrocyclic chelator which is attached tothe Albumin fusion protein of the invention is1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetic acid (DOTA). Inother specific embodiments, the DOTA is attached to the Albumin fusionprotein of the invention via a linker molecule. Examples of linkermolecules useful for conjugating DOTA to a polypeptide are commonlyknown in the art—see, for example, DeNardo et al., Clin. Cancer Res.4(10):2483-90, 1998; Peterson et al., Bioconjug. Chem. 10(4):553-7,1999; and Zimmerman et al., Nucl. Med. Biol. 26(8):943-50, 1999 whichare hereby incorporated by reference in their entirety. In addition,U.S. Pat. Nos. 5,652,361 and 5,756,065, which disclose chelating agentsthat may be conjugated to antibodies, and methods for making and usingthem, are hereby incorporated by reference in their entireties. ThoughU.S. Pat. Nos. 5,652,361 and 5,756,065 focus on conjugating chelatingagents to antibodies, one skilled in the art could readily adapt themethod disclosed therein in order to conjugate chelating agents to otherpolypeptides.

Bifunctional chelators based on macrocyclic ligands in which conjugationis via an activated arm, or functional group, attached to the carbonbackbone of the ligand can be employed as described by M. Moi et al., J.Amer. Chem. Soc. 49:2639 (1989)(2-p-nitrobenzyl-1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraaceticacid); S. V. Deshpande et al., J. Nucl. Med. 31:473 (1990); G. Ruser etal., Bioconj. Chem. 1:345 (1990); C. J. Broan et al., J. C. S. Chem.Comm. 23:1739 (1990); and C. J. Anderson et al., J. Nucl. Med. 36:850(1995).

In one embodiment, a macrocyclic chelator, such as polyazamacrocyclicchelators, optionally containing one or more carboxy, amino,hydroxamate, phosphonate, or phosphate groups, are attached to theAlbumin fusion protein of the invention. In another embodiment, thechelator is a chelator selected from the group consisting of DOTA,analogues of DOTA, and derivatives of DOTA.

In one embodiment, suitable chelator molecules that may be attached tothe the Albumin fusion protein of the invention include DOXA(1-oxa-4,7,10-triazacyclododecanetriacetic acid), NOTA(1,4,7-triazacyclononanetriacetic acid), TETA(1,4,8,11-tetraazacyclotetradecanetetraacetic acid), and THT(4′-(3-amino-4-methoxy-phenyl)-6,6″-bis(N′,N′-dicarboxymethyl-N-methylhydrazino)-2,2′:6′,2″-terpyridine),and analogs and derivatives thereof. See, e.g., Ohmono et al., J. Med.Chem. 35: 157-162 (1992); Kung et al., J. Nucl. Med. 25: 326-332 (1984);Jurisson et al., Chem. Rev. 93:1137-1156 (1993); and U.S. Pat. No.5,367,080. Other suitable chelators include chelating agents disclosedin U.S. Pat. Nos. 4,647,447; 4,687,659; 4,885,363; EP-A-71564;WO89/00557; and EP-A-232751.

In another embodiment, suitable macrocyclic carboxylic acid chelatorswhich can be used in the present invention include1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetic acid (DOTA);1,4,8,12-tetraazacyclopentadecane-N,N′,N″,N′″-tetraacetic acid (15N4);1,4,7-triazacyclononane-N,N′,N″-triacetic acid (9N3);1,5,9-triazacyclododecane-N,N′,N″-triacetic acid (12N3); and6-bromoacetamido-benzyl-1,4,8,11-tetraazacyclotetradecane-N,N′,N″,N′″-tetraaceticacid (BAT).

A preferred chelator that can be attached to the Albumin Fusion proteinof the invention isα-(5-isothiocyanato-2-methoxyphenyl)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraaceticacid, which is also known as MeO-DOTA-NCS. A salt or ester ofα-(5-isothiocyanato-2-methoxyphenyl)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraaceticacid may also be used.

Albumin fusion proteins of the invention to which chelators such asthose described are covalently attached may be labeled (via thecoordination site of the chelator) with radionuclides that are suitablefor therapeutic, diagnostic, or both therapeutic and diagnosticpurposes. Examples of appropriate metals include Ag, At, Au, Bi, Cu, Ga,Ho, In, Lu, Pb, Pd, Pm, Pr, Rb, Re, Rh, Sc, Sr, Tc, Tl, Y, and Yb.Examples of the radionuclide used for diagnostic purposes are Fe, Gd,¹¹¹In, ⁶⁷Ga, or ⁶⁸Ga. In another embodiment, the radionuclide used fordiagnostic purposes is ¹¹¹In, or ⁶⁷Ga. Examples of the radionuclide usedfor therapeutic purposes are ¹⁶⁶Ho, ¹⁶⁵Dy, ⁹⁰Y, ^(115m)In, ⁵²Fe, or⁷²Ga. In one embodiment, the radionuclide used for diagnostic purposesis ¹⁶⁶Ho or ⁹⁰Y. Examples of the radionuclides used for both therapeuticand diagnostic purposes include ¹⁵³Sm, ¹⁷⁷Lu, ¹⁵⁹Gd, ¹⁷⁵Yb, or ⁴⁷Sc. Inone embodiment, the radionuclide is ¹⁵³Sm, ¹⁷⁷Lu, ¹⁷⁵Yb, or ¹⁵⁹Gd.

Preferred metal radionuclides include ⁹⁰Y, ^(99m)Tc, ¹¹¹In, ⁴⁷Sc, ⁶⁷Ga,⁵¹Cr, ^(177m)Sn, ⁶⁷Cu, ¹⁶⁷Tm, ⁹⁷Ru, ¹⁸⁸Re, ¹⁷⁷Lu, ¹⁹⁹Au, ⁴⁷Sc, ⁶⁷Ga,⁵¹Cr, ^(177m)Sn, ⁶⁷Cu, ¹⁶⁷Tm, ⁹⁵Ru, ¹⁸⁸Re, ¹⁷⁷Lu, ¹⁹⁹Au, ²⁰³Pb and¹⁴¹Ce.

In a particular embodiment, Albumin fusion proteins of the invention towhich chelators are covalently attached may be labeled with a metal ionselected from the group consisting of ⁹⁰Y, ¹¹¹In, ¹⁷⁷Lb, ¹⁶⁶Ho, ²¹⁵Biand ²²⁵Ac.

Moreover, γ-emitting radionuclides, such as ^(99m)Tc, ¹¹¹In, ⁶⁷Ga, and¹⁶⁹Yb have been approved or under investigation for diagnostic imaging,while β-emitters, such as ⁶⁷Cu, ¹¹¹Ag, ¹⁸⁶Re, and ⁹⁰Y are useful for theapplications in tumor therapy. Also other useful radionuclides includeγ-emitters, such as ^(99m)Tc, ¹¹¹In, ⁶⁷Ga, and ¹⁶⁹Yb, and β-emitters,such as ⁶⁷Cu, ¹¹¹Ag, ¹⁸⁶Re, ¹⁸⁸Re, and ⁹⁰Y, as well as otherradionuclides of interest such as ²¹¹At, ²¹²Bi, ¹⁷⁷Lb, ⁸⁶Rb, ¹⁰⁵Rb,¹⁵³Sm, ¹⁹⁸Au, ¹⁴⁹Pm, ⁸⁵Sr, ¹⁴²Pr, ²¹⁴Pb, ¹⁰⁹Pd, ¹⁶⁶Ho, ²⁰⁸Tl, and ⁴⁴Sc.Albumin fusion proteins of the invention to which chelators arecovalently attached may be labeled with the radionuclides describedabove.

In another embodiment, Albumin fusion proteins of the invention to whichchelators are covalently attached may be labeled with paramagnetic metalions including ions of transition and lanthanide metal, such as metalshaving atomic numbers of 21-29, 42, 43, 44, or 57-71, in particular ionsof Cr, V, Mn, Fe, Co, Ni, Cu, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy,Ho, Er, Tm, Yb, and Lu. The paramagnetic metals used in compositions formagnetic resonance imaging include the elements having atomic numbers of22 to 29, 42, 44 and 58-70.

In another embodiment, Albumin fusion proteins of the invention to whichchelators are covalently attached may be labeled with fluorescent metalions including lanthanides, in particular La, Ce, Pr, Nd, Pm, Sm, Eu(e.g., ¹⁵²Eu) Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

In another embodiment, Albumin fusion proteins of the invention to whichchelators are covalently attached may be labeled with heavymetal-containing reporters may include atoms of Mo, Bi, Si, and W.

It is also possible to label the albumin fusion proteins with afluorescent compound. When the fluorescently labeled antibody is exposedto light of the proper wave length, its presence can then be detecteddue to fluorescence. Among the most commonly used fluorescent labelingcompounds are fluorescein isothiocyanate, rhodamine, phycoerythrin,phycocyanin, allophycocyanin, ophthaldehyde and fluorescamine.

The albumin fusion protein can also be detectably labeled usingfluorescence emitting metals such as ¹⁵²Eu, or others of the lanthanideseries. These metals can be attached to the antibody using such metalchelating groups as diethylenetriaminepentacetic acid (DTPA) orethylenediaminetetraacetic acid (EDTA).

The albumin fusion proteins can also can be detectably labeled bycoupling it to a chemiluminescent compound. The presence of thechemiluminescent-tagged albumin fusion protein is then determined bydetecting the presence of luminescence that arises during the course ofa chemical reaction. Examples of particularly useful chemiluminescentlabeling compounds are luminol, isoluminol, theromatic acridinium ester,imidazole, acridinium salt and oxalate ester.

Likewise, a bioluminescent compound may be used to label albumin fusionproteins of the present invention. Bioluminescence is a type ofchemiluminescence found in biological systems in, which a catalyticprotein increases the efficiency of the chemiluminescent reaction. Thepresence of a bioluminescent protein is determined by detecting thepresence of luminescence. Important bioluminescent compounds forpurposes of labeling are luciferin, luciferase and aequorin.

Transgenic Organisms

Transgenic organisms that express the albumin fusion proteins of theinvention are also included in the invention. Transgenic organisms aregenetically modified organisms into which recombinant, exogenous orcloned genetic material has been transferred. Such genetic material isoften referred to as a transgene. The nucleic acid sequence of thetransgene may include one or more transcriptional regulatory sequencesand other nucleic acid sequences such as introns, that may be necessaryfor optimal expression and secretion of the encoded protein. Thetransgene may be designed to direct the expression of the encodedprotein in a manner that facilitates its recovery from the organism orfrom a product produced by the organism, e.g. from the milk, blood,urine, eggs, hair or seeds of the organism. The transgene may consist ofnucleic acid sequences derived from the genome of the same species or ofa different species than the species of the target animal. The transgenemay be integrated either at a locus of a genome where that particularnucleic acid sequence is not otherwise normally found or at the normallocus for the transgene.

The term “germ cell line transgenic organism” refers to a transgenicorganism in which the genetic alteration or genetic information wasintroduced into a germ line cell, thereby conferring the ability of thetransgenic organism to transfer the genetic information to offspring. Ifsuch offspring in fact possess some or all of that alteration or geneticinformation, then they too are transgenic organisms. The alteration orgenetic information may be foreign to the species of organism to whichthe recipient belongs, foreign only to the particular individualrecipient, or may be genetic information already possessed by therecipient. In the last case, the altered or introduced gene may beexpressed differently than the native gene.

A transgenic organism may be a transgenic animal or a transgenic plant.Transgenic animals can be produced by a variety of different methodsincluding transfection, electroporation, microinjection, gene targetingin embryonic stem cells and recombinant viral and retroviral infection(see, e.g., U.S. Pat. No. 4,736,866; U.S. Pat. No. 5,602,307; Mullins etal. (1993) Hypertension 22(4):630-633; Brenin et al. (1997) Surg. Oncol.6(2)99-110; Tuan (ed.), Recombinant Gene Expression Protocols, Methodsin Molecular Biology No. 62, Humana Press (1997)). The method ofintroduction of nucleic acid fragments into recombination competentmammalian cells can be by any method which favors co-transformation ofmultiple nucleic acid molecules. Detailed procedures for producingtransgenic animals are readily available to one skilled in the art,including the disclosures in U.S. Pat. No. 5,489,743 and U.S. Pat. No.5,602,307.

A number of recombinant or transgenic mice have been produced, includingthose which express an activated oncogene sequence (U.S. Pat. No.4,736,866); express simian SV40 T-antigen (U.S. Pat. No. 5,728,915);lack the expression of interferon regulatory factor 1 (IRF-1) (U.S. Pat.No. 5,731,490); exhibit dopaminergic dysfunction (U.S. Pat. No.5,723,719); express at least one human gene which participates in bloodpressure control (U.S. Pat. No. 5,731,489); display greater similarityto the conditions existing in naturally occurring Alzheimer's disease(U.S. Pat. No. 5,720,936); have a reduced capacity to mediate cellularadhesion (U.S. Pat. No. 5,602,307); possess a bovine growth hormone gene(Clutter et al. (1996) Genetics 143(4):1753-1760); or, are capable ofgenerating a fully human antibody response (McCarthy (1997) The Lancet349(9049):405).

While mice and rats remain the animals of choice for most transgenicexperimentation, in some instances it is preferable or even necessary touse alternative animal species. Transgenic procedures have beensuccessfully utilized in a variety of non-murine animals, includingsheep, goats, pigs, dogs, cats, monkeys, chimpanzees, hamsters, rabbits,cows and guinea pigs (see, e.g., Kim et al. (1997) Mol. Reprod. Dev.46(4):515-526; Houdebine (1995) Reprod. Nutr. Dev. 35(6):609-617;Petters (1994) Reprod. Fertil. Dev. 6(5):643-645; Schnieke et al. (1997)Science 278(5346):2130-2133; and Amoah (1997) J. Animal Science75(2):578-585).

To direct the secretion of the transgene-encoded protein of theinvention into the milk of transgenic mammals, it may be put under thecontrol of a promoter that is preferentially activated in mammaryepithelial cells. Promoters that control the genes encoding milkproteins are preferred, for example the promoter for casein, betalactoglobulin, whey acid protein, or lactalbumin (see, e.g., DiTullio(1992) BioTechnology 10:74-77; Clark et al. (1989) BioTechnology7:487-492; Gorton et al. (1987) BioTechnology 5:1183-1187; and Soulieret al. (1992) FEBS Letts. 297:13). The transgenic mammals of choicewould produce large volumes of milk and have long lactating periods, forexample goats, cows, camels or sheep.

An albumin fusion protein of the invention can also be expressed in atransgenic plant, e.g. a plant in which the DNA transgene is insertedinto the nuclear or plastidic genome. Plant transformation proceduresused to introduce foreign nucleic acids into plant cells or protoplastsare known in the art. See, in general, Methods in Enzymology Vol. 153(“Recombinant DNA Part D”) 1987, Wu and Grossman Eds., Academic Pressand European Patent Application EP 693554. Methods for generation ofgenetically engineered plants are further described in U.S. Pat. No.5,283,184, U.S. Pat. No. 5,482,852, and European Patent Application EP693 554, all of which are hereby incorporated by reference.

Pharmaceutical or Therapeutic Compositions

The albumin fusion proteins of the invention or formulations thereof maybe administered by any conventional method including parenteral (e.g.subcutaneous or intramuscular) injection or intravenous infusion. Thetreatment may consist of a single dose or a plurality of doses over aperiod of time.

While it is possible for an albumin fusion protein of the invention tobe administered alone, it is preferable to present it as apharmaceutical formulation, together with one or more acceptablecarriers. The carrier(s) must be “acceptable” in the sense of beingcompatible with the albumin fusion protein and not deleterious to therecipients thereof. Typically, the carriers will be water or salinewhich will be sterile and pyrogen free. Albumin fusion proteins of theinvention are particularly well suited to formulation in aqueouscarriers such as sterile pyrogen free water, saline or other isotonicsolutions because of their extended shelf-life in solution. Forinstance, pharmaceutical compositions of the invention may be formulatedwell in advance in aqueous form, for instance, weeks or months or longertime periods before being dispensed.

For example, formulations containing the albumin fusion protein may beprepared taking into account the extended shelf-life of the albuminfusion protein in aqueous formulations. As discussed above, theshelf-life of many of these Therapeutic proteins are markedly increasedor prolonged after fusion to HA.

In instances where aerosol administration is appropriate, the albuminfusion proteins of the invention can be formulated as aerosols usingstandard procedures. The term “aerosol” includes any gas-borne suspendedphase of an albumin fusion protein of the instant invention which iscapable of being inhaled into the bronchioles or nasal passages.Specifically, aerosol includes a gas-borne suspension of droplets of analbumin fusion protein of the instant invention, as may be produced in ametered dose inhaler or nebulizer, or in a mist sprayer. Aerosol alsoincludes a dry powder composition of a compound of the instant inventionsuspended in air or other carrier gas, which may be delivered byinsufflation from an inhaler device, for example. See Ganderton & Jones,Drug Delivery to the Respiratory Tract, Ellis Horwood (1987); Gonda(1990) Critical Reviews in Therapeutic Drug Carrier Systems 6:273-313;and Raeburn et al., (1992) Pharmacol. Toxicol. Methods 27:143-159.

The formulations of the invention are also typically non-immunogenic, inpart, because of the use of the components of the albumin fusion proteinbeing derived from the proper species. For instance, for human use, boththe Therapeutic protein and albumin portions of the albumin fusionprotein will typically be human. In some cases, wherein either componentis non human-derived, that component may be humanized by substitution ofkey amino acids so that specific epitopes appear to the human immunesystem to be human in nature rather than foreign.

The formulations may conveniently be presented in unit dosage form andmay be prepared by any of the methods well known in the art of pharmacy.Such methods include the step of bringing into association the albuminfusion protein with the carrier that constitutes one or more accessoryingredients. In general the formulations are prepared by uniformly andintimately bringing into association the active ingredient with liquidcarriers or finely divided solid carriers or both, and then, ifnecessary, shaping the product.

Formulations suitable for parenteral administration include aqueous andnon-aqueous sterile injection solutions which may contain anti-oxidants,buffers, bacteriostats and solutes which render the formulationappropriate for the intended recipient; and aqueous and non-aqueoussterile suspensions which may include suspending agents and thickeningagents. The formulations may be presented in unit-dose or multi-dosecontainers, for example sealed ampules, vials or syringes, and may bestored in a freeze-dried (lyophilised) condition requiring only theaddition of the sterile liquid carrier, for example water forinjections, immediately prior to use. Extemporaneous injection solutionsand suspensions may be prepared from sterile powders. Dosageformulations may contain the Therapeutic protein portion at a lowermolar concentration or lower dosage compared to the non-fused standardformulation for the Therapeutic protein given the extended serumhalf-life exhibited by many of the albumin fusion proteins of theinvention.

As an example, when an albumin fusion protein of the invention comprisesone of the proteins listed in the “Therapeutic Protein:X” column ofTable 1 as one or more of the Therapeutic protein regions, the dosageform can be calculated on the basis of the potency of the albumin fusionprotein relative to the potency of hGH, while taking into account theprolonged serum half-life and shelf-life of the albumin fusion proteinscompared to that of native hGH. Growth hormone is typically administeredat 0.3 to 30.0 IU/kg/week, for example 0.9 to 12.0 IU/kg/week, given inthree or seven divided doses for a year or more. In an albumin fusionprotein consisting of full length HA fused to full length GH, anequivalent dose in terms of units would represent a greater weight ofagent but the dosage frequency can be reduced, for example to twice aweek, once a week or less.

Formulations or compositions of the invention may be packaged togetherwith, or included in a kit with, instructions or a package insertreferring to the extended shelf-life of the albumin fusion proteincomponent. For instance, such instructions or package inserts mayaddress recommended storage conditions, such as time, temperature andlight, taking into account the extended or prolonged shelf-life of thealbumin fusion proteins of the invention. Such instructions or packageinserts may also address the particular advantages of the albumin fusionproteins of the inventions, such as the ease of storage for formulationsthat may require use in the field, outside of controlled hospital,clinic or office conditions. As described above, formulations of theinvention may be in aqueous form and may be stored under less than idealcircumstances without significant loss of therapeutic activity.

Albumin fusion proteins of the invention can also be included innutraceuticals. For instance, certain albumin fusion proteins of theinvention may be administered in natural products, including milk ormilk product obtained from a transgenic mammal which expresses albuminfusion protein. Such compositions can also include plant or plantproducts obtained from a transgenic plant which expresses the albuminfusion protein. The albumin fusion protein can also be provided inpowder or tablet form, with or without other known additives, carriers,fillers and diluents. Nutraceuticals are described in Scott Hegenhart,Food Product Design, December 1993.

The invention also provides methods of treatment and/or prevention ofdiseases or disorders (such as, for example, any one or more of thediseases or disorders disclosed herein) by administration to a subjectof an effective amount of an albumin fusion protein of the invention ora polynucleotide encoding an albumin fusion protein of the invention(“albumin fusion polynucleotide”) in a pharmaceutically acceptablecarrier.

The albumin fusion protein and/or polynucleotide will be formulated anddosed in a fashion consistent with good medical practice, taking intoaccount the clinical condition of the individual patient (especially theside effects of treatment with the albumin fusion protein and/orpolynucleotide alone), the site of delivery, the method ofadministration, the scheduling of administration, and other factorsknown to practitioners. The “effective amount” for purposes herein isthus determined by such considerations.

As a general proposition, the total pharmaceutically effective amount ofthe albumin fusion protein administered parenterally per dose will be inthe range of about lug/kg/day to 10 mg/kg/day of patient body weight,although, as noted above, this will be subject to therapeuticdiscretion. More preferably, this dose is at least 0.01 mg/kg/day, andmost preferably for humans between about 0.01 and 1 mg/kg/day for thehormone. If given continuously, the albumin fusion protein is typicallyadministered at a dose rate of about 1 ug/kg/hour to about 50ug/kg/hour, either by 1-4 injections per day or by continuoussubcutaneous infusions, for example, using a mini-pump. An intravenousbag solution may also be employed. The length of treatment needed toobserve changes and the interval following treatment for responses tooccur appears to vary depending on the desired effect.

Albumin fusion proteins and/or polynucleotides can be are administeredorally, rectally, parenterally, intracisternally, intravaginally,intraperitoneally, topically (as by powders, ointments, gels, drops ortransdermal patch), bucally, or as an oral or nasal spray.“Pharmaceutically acceptable carrier” refers to a non-toxic solid,semisolid or liquid filler, diluent, encapsulating material orformulation auxiliary of any. The term “parenteral” as used hereinrefers to modes of administration which include intravenous,intramuscular, intraperitoneal, intrasternal, subcutaneous andintraarticular injection and infusion.

Albumin fusion proteins and/or polynucleotides of the invention are alsosuitably administered by sustained-release systems. Examples ofsustained-release albumin fusion proteins and/or polynucleotides areadministered orally, rectally, parenterally, intracisternally,intravaginally, intraperitoneally, topically (as by powders, ointments,gels, drops or transdermal patch), bucally, or as an oral or nasalspray. “Pharmaceutically acceptable carrier” refers to a non-toxicsolid, semisolid or liquid filler, diluent, encapsulating material orformulation auxiliary of any type. The term “parenteral” as used hereinrefers to modes of administration which include intravenous,intramuscular, intraperitoneal, intrasternal, subcutaneous andintraarticular injection and infusion. Additional examples ofsustained-release albumin fusion proteins and/or polynucleotides includesuitable polymeric materials (such as, for example, semi-permeablepolymer matrices in the form of shaped articles, e.g., films, ormicrocapsules), suitable hydrophobic materials (for example as anemulsion in an acceptable oil) or ion exchange resins, and sparinglysoluble derivatives (such as, for example, a sparingly soluble salt).

Sustained-release matrices include polylactides (U.S. Pat. No.3,773,919, EP 58,481), copolymers of L-glutamic acid andgamma-ethyl-L-glutamate (Sidman et al., Biopolymers 22:547-556 (1983)),poly(2-hydroxyethyl methacrylate) (Langer et al., J. Biomed. Mater. Res.15:167-277 (1981), and Langer, Chem. Tech. 12:98-105 (1982)), ethylenevinyl acetate (Langer et al., Id.) or poly-D-(−)-3-hydroxybutyric acid(EP 133,988).

Sustained-release albumin fusion proteins and/or polynucleotides alsoinclude liposomally entrapped albumin fusion proteins and/orpolynucleotides of the invention (see generally, Langer, Science249:1527-1533 (1990); Treat et al., in Liposomes in the Therapy ofInfectious Disease and Cancer, Lopez-Berestein and Fidler (eds.), Liss,New York, pp. 317-327 and 353-365 (1989)). Liposomes containing thealbumin fusion protein and/or polynucleotide are prepared by methodsknown per se: DE 3,218,121; Epstein et al., Proc. Natl. Acad. Sci. (USA)82:3688-3692 (1985); Hwang et al., Proc. Natl. Acad. Sci.(USA)77:4030-4034 (1980); EP 52,322; EP 36,676; EP 88,046; EP 143,949; EP142,641; Japanese Pat. Appl. 83-118008; U.S. Pat. Nos. 4,485,045 and4,544,545; and EP 102,324. Ordinarily, the liposomes are of the small(about 200-800 Angstroms) unilamellar type in which the lipid content isgreater than about 30 mol. percent cholesterol, the selected proportionbeing adjusted for the optimal Therapeutic.

In yet an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are delivered by way of a pump (seeLanger, supra; Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987);Buchwald et al., Surgery 88:507 (1980); Saudek et al., N. Engl. J. Med.321:574 (1989)).

Other controlled release systems are discussed in the review by Langer(Science 249:1527-1533 (1990)).

For parenteral administration, in one embodiment, the albumin fusionprotein and/or polynucleotide is formulated generally by mixing it atthe desired degree of purity, in a unit dosage injectable form(solution, suspension, or emulsion), with a pharmaceutically acceptablecarrier, i.e., one that is non-toxic to recipients at the dosages andconcentrations employed and is compatible with other ingredients of theformulation. For example, the formulation preferably does not includeoxidizing agents and other compounds that are known to be deleterious tothe Therapeutic.

Generally, the formulations are prepared by contacting the albuminfusion protein and/or polynucleotide uniformly and intimately withliquid carriers or finely divided solid carriers or both. Then, ifnecessary, the product is shaped into the desired formulation.Preferably the carrier is a parenteral carrier, more preferably asolution that is isotonic with the blood of the recipient. Examples ofsuch carrier vehicles include water, saline, Ringer's solution, anddextrose solution. Non-aqueous vehicles such as fixed oils and ethyloleate are also useful herein, as well as liposomes.

The carrier suitably contains minor amounts of additives such assubstances that enhance isotonicity and chemical stability. Suchmaterials are non-toxic to recipients at the dosages and concentrationsemployed, and include buffers such as phosphate, citrate, succinate,acetic acid, and other organic acids or their salts; antioxidants suchas ascorbic acid; low molecular weight (less than about ten residues)polypeptides, e.g., polyarginine or tripeptides; proteins, such as serumalbumin, gelatin, or immunoglobulins; hydrophilic polymers such aspolyvinylpyrrolidone; amino acids, such as glycine, glutamic acid,aspartic acid, or arginine; monosaccharides, disaccharides, and othercarbohydrates including cellulose or its derivatives, glucose, manose,or dextrins; chelating agents such as EDTA; sugar alcohols such asmannitol or sorbitol; counterions such as sodium; and/or nonionicsurfactants such as polysorbates, poloxamers, or PEG.

The albumin fusion protein is typically formulated in such vehicles at aconcentration of about 0.1 mg/ml to 100 mg/ml, preferably 1-10 mg/ml, ata pH of about 3 to 8. It will be understood that the use of certain ofthe foregoing excipients, carriers, or stabilizers will result in theformation of polypeptide salts.

Any pharmaceutical used for therapeutic administration can be sterile.Sterility is readily accomplished by filtration through sterilefiltration membranes (e.g., 0.2 micron membranes). Albumin fusionproteins and/or polynucleotides generally are placed into a containerhaving a sterile access port, for example, an intravenous solution bagor vial having a stopper pierceable by a hypodermic injection needle.

Albumin fusion proteins and/or polynucleotides ordinarily will be storedin unit or multi-dose containers, for example, sealed ampoules or vials,as an aqueous solution or as a lyophilized formulation forreconstitution. As an example of a lyophilized formulation, 10-ml vialsare filled with 5 ml of sterile-filtered 1% (w/v) aqueous albumin fusionprotein and/or polynucleotide solution, and the resulting mixture islyophilized. The infusion solution is prepared by reconstituting thelyophilized albumin fusion protein and/or polynucleotide usingbacteriostatic Water-for-Injection.

In a specific and preferred embodiment, the Albumin fusion proteinformulations comprises 0.01 M sodium phosphate, 0.15 mM sodium chloride,0.16 micromole sodium octanoate/milligram of fusion protein, 15micrograms/milliliter polysorbate 80, pH 7.2. In another specific andpreferred embodiment, the Albumin fusion protein formulations consists0.01 M sodium phosphate, 0.15 mM sodium chloride, 0.16 micromole sodiumoctanoate/milligram of fusion protein, 15 micrograms/milliliterpolysorbate 80, pH 7.2. The pH and buffer are chosen to matchphysiological conditions and the salt is added as a tonicifier. Sodiumoctanoate has been chosen due to its reported ability to increase thethermal stability of the protein in solution. Finally, polysorbate hasbeen added as a generic surfactant, which lowers the surface tension ofthe solution and lowers non-specific adsorption of the albumin fusionprotein to the container closure system.

The invention also provides a pharmaceutical pack or kit comprising oneor more containers filled with one or more of the ingredients of thealbumin fusion proteins and/or polynucleotides of the invention.Associated with such container(s) can be a notice in the form prescribedby a governmental agency regulating the manufacture, use or sale ofpharmaceuticals or biological products, which notice reflects approvalby the agency of manufacture, use or sale for human administration. Inaddition, the albumin fusion proteins and/or polynucleotides may beemployed in conjunction with other therapeutic compounds.

The albumin fusion proteins and/or polynucleotides of the invention maybe administered alone or in combination with adjuvants. Adjuvants thatmay be administered with the albumin fusion proteins and/orpolynucleotides of the invention include, but are not limited to, alum,alum plus deoxycholate (ImmunoAg), MTP-PE (Biocine Corp.), QS21(Genentech, Inc.), BCG (e.g., THERACYS®), MPL and nonviable preparationsof Corynebacterium parvum. In a specific embodiment, albumin fusionproteins and/or polynucleotides of the invention are administered incombination with alum. In another specific embodiment, albumin fusionproteins and/or polynucleotides of the invention are administered incombination with QS-21. Further adjuvants that may be administered withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, Monophosphoryl lipid immunomodulator,AdjuVax 100a, QS-21, QS-18, CRL1005, Aluminum salts, MF-59, andVirosomal adjuvant technology. Vaccines that may be administered withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, vaccines directed toward protectionagainst MMR (measles, mumps, rubella), polio, varicella,tetanus/diptheria, hepatitis A, hepatitis B, Haemophilus influenzae B,whooping cough, pneumonia, influenza, Lyme's Disease, rotavirus,cholera, yellow fever, Japanese encephalitis, poliomyelitis, rabies,typhoid fever, and pertussis. Combinations may be administered eitherconcomitantly, e.g., as an admixture, separately but simultaneously orconcurrently; or sequentially. This includes presentations in which thecombined agents are administered together as a therapeutic mixture, andalso procedures in which the combined agents are administered separatelybut simultaneously, e.g., as through separate intravenous lines into thesame individual. Administration “in combination” further includes theseparate administration of one of the compounds or agents given first,followed by the second.

The albumin fusion proteins and/or polynucleotides of the invention maybe administered alone or in combination with other therapeutic agents.Albumin fusion protein and/or polynucleotide agents that may beadministered in combination with the albumin fusion proteins and/orpolynucleotides of the invention, include but not limited to,chemotherapeutic agents, antibiotics, steroidal and non-steroidalanti-inflammatories, conventional immunotherapeutic agents, and/ortherapeutic treatments described below. Combinations may be administeredeither concomitantly, e.g., as an admixture, separately butsimultaneously or concurrently; or sequentially. This includespresentations in which the combined agents are administered together asa therapeutic mixture, and also procedures in which the combined agentsare administered separately but simultaneously, e.g., as throughseparate intravenous lines into the same individual. Administration “incombination” further includes the separate administration of one of thecompounds or agents given first, followed by the second.

In one embodiment, the albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with an anticoagulant.Anticoagulants that may be administered with the compositions of theinvention include, but are not limited to, heparin, low molecular weightheparin, warfarin sodium (e.g., COUMADIN®), dicumarol,4-hydroxycoumarin, anisindione (e.g., MIRADON™), acenocoumarol (e.g.,nicoumalone, SINTHROME™), indan-1,3-dione, phenprocoumon (e.g.,MARCUMAR™), ethyl biscoumacetate (e.g., TROMEXAN™), and aspirin. In aspecific embodiment, compositions of the invention are administered incombination with heparin and/or warfarin. In another specificembodiment, compositions of the invention are administered incombination with warfarin. In another specific embodiment, compositionsof the invention are administered in combination with warfarin andaspirin. In another specific embodiment, compositions of the inventionare administered in combination with heparin. In another specificembodiment, compositions of the invention are administered incombination with heparin and aspirin.

In another embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withthrombolytic drugs. Thrombolytic drugs that may be administered with thecompositions of the invention include, but are not limited to,plasminogen, lys-plasminogen, alpha2-antiplasmin, streptokinae (e.g.,KABIKINASE™) antiresplace (e.g., EMINASE™), tissue plasminogen activator(t-PA, altevase, ACTIVASE™), urokinase (e.g., ABBOKINASE™), sauruplase,(Prourokinase, single chain urokinase), and aminocaproic acid (e.g.,AMICAR™). In a specific embodiment, compositions of the invention areadministered in combination with tissue plasminogen activator andaspirin.

In another embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withantiplatelet drugs. Antiplatelet drugs that may be administered with thecompositions of the invention include, but are not limited to, aspirin,dipyridamole (e.g., PERSANTINE™), and ticlopidine (e.g., TICLID™).

In specific embodiments, the use of anti-coagulants, thrombolytic and/orantiplatelet drugs in combination with albumin fusion proteins and/orpolynucleotides of the invention is contemplated for the prevention,diagnosis, and/or treatment of thrombosis, arterial thrombosis, venousthrombosis, thromboembolism, pulmonary embolism, atherosclerosis,myocardial infarction, transient ischemic attack, unstable angina. Inspecific embodiments, the use of anticoagulants, thrombolytic drugsand/or antiplatelet drugs in combination with albumin fusion proteinsand/or polynucleotides of the invention is contemplated for theprevention of occlusion of saphenous grafts, for reducing the risk ofperiprocedural thrombosis as might accompany angioplasty procedures, forreducing the risk of stroke in patients with atrial fibrillationincluding nonrheumatic atrial fibrillation, for reducing the risk ofembolism associated with mechanical heart valves and or mitral valvesdisease. Other uses for the therapeutics of the invention, alone or incombination with antiplatelet, anticoagulant, and/or thrombolytic drugs,include, but are not limited to, the prevention of occlusions inextracorporeal devices (e.g., intravascular cannulas, vascular accessshunts in hemodialysis patients, hemodialysis machines, andcardiopulmonary bypass machines).

In certain embodiments, albumin fusion proteins and/or polynucleotidesof the invention are administered in combination with antiretroviralagents, nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs),non-nucleoside reverse transcriptase inhibitors (NNRTIs), and/orprotease inhibitors (PIs). NRTIs that may be administered in combinationwith the albumin fusion proteins and/or polynucleotides of theinvention, include, but are not limited to, RETROVIR™ (zidovudine/AZT),VIDEX™ (didanosine/ddI), HIVID™ (zalcitabine/ddC), ZERIT™(stavudine/d4T), EPIVIR™ (lamivudine/3TC), and COMBIVIR™(zidovudine/lamivudine). NNRTIs that may be administered in combinationwith the albumin fusion proteins and/or polynucleotides of theinvention, include, but are not limited to, VIRAIVIUNE™ (nevirapine),RESCRIPTOR™ (delavirdine), and SUSTIVA™ (efavirenz). Protease inhibitorsthat may be administered in combination with the albumin fusion proteinsand/or polynucleotides of the invention, include, but are not limitedto, CRIXIVAN™ (indinavir), NORVIR™ (ritonavir), INVIRASE™ (saquinavir),and VIRACEPT™ (nelfinavir). In a specific embodiment, antiretroviralagents, nucleoside reverse transcriptase inhibitors, non-nucleosidereverse transcriptase inhibitors, and/or protease inhibitors may be usedin any combination with albumin fusion proteins and/or polynucleotidesof the invention to treat AIDS and/or to prevent or treat HIV infection.

Additional NRTIs include LODENOSINE™ (F-ddA; an acid-stable adenosineNRTI; Triangle/Abbott; COVIRACIL™ (emtricitabine/FTC; structurallyrelated to lamivudine (3TC) but with 3- to 10-fold greater activity invitro; Triangle/Abbott); dOTC (BCH-10652, also structurally related tolamivudine but retains activity against a substantial proportion oflamivudine-resistant isolates; Biochem Pharma); Adefovir (refusedapproval for anti-HIV therapy by FDA; Gilead Sciences); PREVEON®(Adefovir Dipivoxil, the active prodrug of adefovir; its active form isPMEA-pp); TENOFOVIR™ (bis-POC PMPA, a PMPA prodrug; Gilead); DAPD/DXG(active metabolite of DAPD; Triangle/Abbott); D-D4FC (related to 3TC,with activity against AZT/3TC-resistant virus); GW420867X (GlaxoWellcome); ZIAGEN™ (abacavir/159U89; Glaxo Wellcome Inc.); CS-87(3′azido-2′,3′-dideoxyuridine; WO 99/66936); and S-acyl-2-thioethyl(SATE)-bearing prodrug forms of β-L-FD4C and β-L-FddC (WO 98/17281).

Additional NNRTIs include COACTINON™ (Emivirine/MKC-442, potent NNRTI ofthe HEPT class; Triangle/Abbott); CAPRAVIRINE™ (AG-1549/S-1153, a nextgeneration NNRTI with activity against viruses containing the K103Nmutation; Agouron); PNU-142721 (has 20- to 50-fold greater activity thanits predecessor delavirdine and is active against K103N mutants;Pharmacia & Upjohn); DPC-961 and DPC-963 (second-generation derivativesof efavirenz, designed to be active against viruses with the K103Nmutation; DuPont); GW-420867X (has 25-fold greater activity than HBY097and is active against K103N mutants; Glaxo Wellcome); CALANOLIDE A(naturally occurring agent from the latex tree; active against virusescontaining either or both the Y181C and K103N mutations); and Propolis(WO 99/49830).

Additional protease inhibitors include LOPINAVIR™ (ABT378/r; AbbottLaboratories); BMS-232632 (an azapeptide; Bristol-Myres Squibb);TIPRANAVIR™ (PNU-140690, a non-peptic dihydropyrone; Pharmacia &Upjohn); PD-178390 (a nonpeptidic dihydropyrone; Parke-Davis); BMS232632 (an azapeptide; Bristol-Myers Squibb); L-756,423 (an indinaviranalog; Merck); DMP-450 (a cyclic urea compound; Avid & DuPont); AG-1776(a peptidomimetic with in vitro activity against proteaseinhibitor-resistant viruses; Agouron); VX-175/GW-433908 (phosphateprodrug of amprenavir; Vertex & Glaxo Welcome); CGP61755 (Ciba); andAGENERASE™ (amprenavir; Glaxo Wellcome Inc.).

Additional antiretroviral agents include fusion inhibitors/gp41 binders.Fusion inhibitors/gp41 binders include T-20 (a peptide from residues643-678 of the HIV gp41 transmembrane protein ectodomain which binds togp41 in its resting state and prevents transformation to the fusogenicstate; Trimeris) and T-1249 (a second-generation fusion inhibitor;Trimeris).

Additional antiretroviral agents include fusion inhibitors/chemokinereceptor antagonists. Fusion inhibitors/chemokine receptor antagonistsinclude CXCR4 antagonists such as AMD 3100 (a bicyclam), SDF-1 and itsanalogs, and ALX40-4C (a cationic peptide), T22 (an 18 amino acidpeptide; Trimeris) and the T22 analogs T134 and T140; CCR5 antagonistssuch as RANTES (9-68), AOP-RANTES, NNY-RANTES, and TAK-779; andCCR5/CXCR4 antagonists such as NSC 651016 (a distamycin analog). Alsoincluded are CCR2B, CCR3, and CCR6 antagonists. Chemokine receptoragonists such as RANTES, SDF-1, MIP-1α, MIP-1β, etc., may also inhibitfusion.

Additional antiretroviral agents include integrase inhibitors. Integraseinhibitors include dicaffeoylquinic (DFQA) acids; L-chicoric acid (adicaffeoyltartaric (DCTA) acid); quinalizarin (QLC) and relatedanthraquinones; ZINTEVIR™ (AR 177, an oligonucleotide that probably actsat cell surface rather than being a true integrase inhibitor; Arondex);and naphthols such as those disclosed in WO 98/50347.

Additional antiretroviral agents include hydroxyurea-like compounds suchas BCX-34 (a purine nucleoside phosphorylase inhibitor; Biocryst);ribonucleotide reductase inhibitors such as DIDOX™ (Molecules forHealth); inosine monophosphate dehydrogenase (IMPDH) inhibitors sucha asVX-497 (Vertex); and mycopholic acids such as CellCept (mycophenolatemofetil; Roche).

Additional antiretroviral agents include inhibitors of viral integrase,inhibitors of viral genome nuclear translocation such as arylenebis(methylketone) compounds; inhibitors of HIV entry such as AOP-RANTES,NNY-RANTES, RANTES-IgG fusion protein, soluble complexes of RANTES andglycosaminoglycans (GAG), and AMD-3100; nucleocapsid zinc fingerinhibitors such as dithiane compounds; targets of HIV Tat and Rev; andpharmacoenhancers such as ABT-378.

Other antiretroviral therapies and adjunct therapies include cytokinesand lymphokines such as MIP-1α, MIP-1β, SDF-1α, IL-2, PROLEUKIN™(aldesleukin/L2-7001; Chiron), IL-4, IL-10, IL-12, and IL-13;interferons such as IFN-alpha2a, IFN-alpha2b, or IFN-beta; antagonistsof TNFs, NFκB, GM-CSF, M-CSF, and IL-10; agents that modulate immuneactivation such as cyclosporin and prednisone; vaccines such as Remune™(HIV Immunogen), APL 400-003 (Apollon), recombinant gp120 and fragments,bivalent (B/E) recombinant envelope glycoprotein, rgp120CM235, MNrgp120, SF-2 rgp120, gp120/soluble CD4 complex, Delta JR-FL protein,branched synthetic peptide derived from discontinuous gp120 C3/C4domain, fusion-competent immunogens, and Gag, Pol, Nef, and Tatvaccines; gene-based therapies such as genetic suppressor elements(GSEs; WO 98/54366), and intrakines (genetically modified CC chemokinestargeted to the ER to block surface expression of newly synthesized CCR5(Yang et al., PNAS 94:11567-72 (1997); Chen et al., Nat. Med. 3:1110-16(1997)); antibodies such as the anti-CXCR4 antibody 12G5, the anti-CCR5antibodies 2D7, 5C7, PA8, PA9, PA10, PA11, PA12, and PA14, the anti-CD4antibodies Q4120 and RPA-T4, the anti-CCR3 antibody 7B11, the anti-gp120antibodies 17b, 48d, 447-52D, 257-D, 268-D and 50.1, anti-Tatantibodies, anti-TNF-α antibodies, and monoclonal antibody 33A; arylhydrocarbon (AH) receptor agonists and antagonists such as TCDD,3,3′,4,4′,5-pentachlorobiphenyl, 3,3′,4,4′-tetrachlorobiphenyl, andα-naphthoflavone (WO 98/30213); and antioxidants such asγ-L-glutamyl-L-cysteine ethyl ester (γ-GCE; WO 99/56764).

In a further embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination with anantiviral agent. Antiviral agents that may be administered with thealbumin fusion proteins and/or polynucleotides of the invention include,but are not limited to, acyclovir, ribavirin, amantadine, remantidine,maxamine, or thymalfasin. Specifically, interferon albumin fusionprotein can be administered in combination with any of these agents.Moreover, interferon alpha albumin fusion protein can also beadministered with any of these agents, and preferably, interferon alpha2a or 2b albumin fusion protein can be administered with any of theseagents. Furthermore, interferon beta albumin fusion protein can also beadministered with any of these agents. Additionally, any of the IFNhybrids albumin fusion proteins can be administered in combination withany of these agents.

In a most preferred embodiment, interferon albumin fusion protein isadministered in combination with ribavirin. In a further preferredembodiment, interferon alpha albumin fusion protein is administered incombination with ribavirin. In a further preferred embodiment,interferon alpha 2a albumin fusion protein is administered incombination with ribavirin. In a further preferred embodiment,interferon alpha 2b albumin fusion protein is administered incombination with ribavirin. In a further preferred embodiment,interferon beta albumin fusion protein is administered in combinationwith ribavirin. In a further preferred embodiment, hybrid interferonalbumin fusion protein is administered in combination with ribavirin.

In other embodiments, albumin fusion proteins and/or polynucleotides ofthe invention may be administered in combination with anti-opportunisticinfection agents. Anti-opportunistic agents that may be administered incombination with the albumin fusion proteins and/or polynucleotides ofthe invention, include, but are not limited to,TRIMETHOPRIM-SULFAMETHOXAZOLE™, DAPSONE™, PENTAMIDINE™, ATOVAQUONE™,ISONIAZID™, RIFAMPIN™, PYRAZINAMIDE™, ETHAMBUTOL™, RIFABUTIN™,CLARITHROMYCIN™, AZITHROMYCIN™, GANCICLOVIR™, FOSCARNET™, CIDOFOVIR™,FLUCONAZOLE™, ITRACONAZOLE™, KETOCONAZOLE™, ACYCLOVIR™, FAMCICOLVIR™,PYRIMETHAMINE™, LEUCOVORIN™, NEUPOGEN™ (filgrastim/G-CSF), and LEUKINE™(sargramostim/GM-CSF). In a specific embodiment, albumin fusion proteinsand/or polynucleotides of the invention are used in any combination withTRIMETHOPRIM-SULFAMETHOXAZOLE™, DAPSONE™, PENTAMIDINE™, and/orATOVAQUONE™ to prophylactically treat or prevent an opportunisticPneumocystis carinii pneumonia infection. In another specificembodiment, albumin fusion proteins and/or polynucleotides of theinvention are used in any combination with ISONIAZID™ RIFAMPIN™,PYRAZINAMIDE™, and/or ETHAMBUTOL™ to prophylactically treat or preventan opportunistic Mycobacterium avium complex infection. In anotherspecific embodiment, albumin fusion proteins and/or polynucleotides ofthe invention are used in any combination with RIFABUTIN™,CLARITHROMYCIN™, and/or AZITHROMYCIN™ to prophylactically treat orprevent an opportunistic Mycobacterium tuberculosis infection. Inanother specific embodiment, albumin fusion proteins and/orpolynucleotides of the invention are used in any combination withGANCICLOVIR™, FOSCARNET™, and/or CIDOFOVIR™ to prophylactically treat orprevent an opportunistic cytomegalovirus infection. In another specificembodiment, albumin fusion proteins and/or polynucleotides of theinvention are used in any combination with FLUCONAZOLE™, ITRACONAZOLE™,and/or KETOCONAZOLE™ to prophylactically treat or prevent anopportunistic fungal infection. In another specific embodiment, albuminfusion proteins and/or polynucleotides of the invention are used in anycombination with ACYCLOVIR™ and/or FAMCICOLVIR™ to prophylacticallytreat or prevent an opportunistic herpes simplex virus type I and/ortype II infection. In another specific embodiment, albumin fusionproteins and/or polynucleotides of the invention are used in anycombination with PYRIMETHAMINE™ and/or LEUCOVORIN™ to prophylacticallytreat or prevent an opportunistic Toxoplasma gondii infection. Inanother specific embodiment, albumin fusion proteins and/orpolynucleotides of the invention are used in any combination withLEUCOVORIN™ and/or NEUPOGEN™ to prophylactically treat or prevent anopportunistic bacterial infection.

In a further embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination with anantibiotic agent. Antibiotic agents that may be administered with thealbumin fusion proteins and/or polynucleotides of the invention include,but are not limited to, amoxicillin, beta-lactamases, aminoglycosides,beta-lactam (glycopeptide), beta-lactamases, Clindamycin,chloramphenicol, cephalosporins, ciprofloxacin, erythromycin,fluoroquinolones, macrolides, metronidazole, penicillins, quinolones,rapamycin, rifampin, streptomycin, sulfonamide, tetracyclines,trimethoprim, trimethoprim-sulfamethoxazole, and vancomycin.

In other embodiments, the albumin fusion proteins and/or polynucleotidesof the invention are administered in combination with immunestimulants.Immunostimulants that may be administered in combination with thealbumin fusion proteins and/or polynucleotides of the invention include,but are not limited to, levamisole (e.g., ERGAMISOL™), isoprinosine(e.g. INOSIPLEX™), interferons (e.g. interferon alpha), and interleukins(e.g., IL-2).

In other embodiments, albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with immunosuppressiveagents.

Immunosuppressive agents that may be administered in combination withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, steroids, cyclosporine, cyclosporineanalogs, cyclophosphamide methylprednisone, prednisone, azathioprine,FK-506, 15-deoxyspergualin, and other immunosuppressive agents that actby suppressing the function of responding T cells. Otherimmunosuppressive agents that may be administered in combination withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, prednisolone, methotrexate,thalidomide, methoxsalen, rapamycin, leflunomide, mizoribine(BREDININ™), brequinar, deoxyspergualin, and azaspirane (SKF 105685),ORTHOCLONE OKT® 3 (muromonab-CD3), SANDIMMUNE™, NEORAL™ SANGDYA™(cyclosporine), PROGRAF® (FK506, tacrolimus), CELLCEPT® (mycophenolatemotefil, of which the active metabolite is mycophenolic acid), IMURAN™(azathioprine), glucocorticosteroids, adrenocortical steroids such asDELTASONE™ (prednisone) and HYDELTRASOL™ (prednisolone), FOLEX™ andMEXATE™ (methotrexate), OXSORALEN-ULTRA™ (methoxsalen) and RAPAMUNE™(sirolimus). In a specific embodiment, immunosuppressants may be used toprevent rejection of organ or bone marrow transplantation.

In an additional embodiment, albumin fusion proteins and/orpolynucleotides of the invention are administered alone or incombination with one or more intravenous immune globulin preparations.Intravenous immune globulin preparations that may be administered withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but not limited to, GAMMAR™, IVEEGAM™, SANDOGLOBULIN™ GAMMAGARDS/D™, ATGAM™ (antithymocyte glubulin), and GAMIMUNE™. In a specificembodiment, albumin fusion proteins and/or polynucleotides of theinvention are administered in combination with intravenous immuneglobulin preparations in transplantation therapy (e.g., bone marrowtransplant).

In another embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered alone or as part of acombination therapy, either in vivo to patients or in vitro to cells,for the treatment of cancer. In a specific embodiment, the albuminfusion proteins, particularly IL-2-albumin fusions, are administeredrepeatedly during passive immunotherapy for cancer, such as adoptivecell transfer therapy for metastatic melanoma as described in Dudley etal. (Science Express, 19 Sep. 2002., at www.scienceexpress.org, herebyincorporated by reference in its entirety).

In certain embodiments, the albumin fusion proteins and/orpolynucleotides of the invention are administered alone or incombination with an anti-inflammatory agent. Anti-inflammatory agentsthat may be administered with the albumin fusion proteins and/orpolynucleotides of the invention include, but are not limited to,corticosteroids (e.g. betamethasone, budesonide, cortisone,dexamethasone, hydrocortisone, methylprednisolone, prednisolone,prednisone, and triamcinolone), nonsteroidal anti-inflammatory drugs(e.g., diclofenac, diflunisal, etodolac, fenoprofen, floctafenine,flurbiprofen, ibuprofen, indomethacin, ketoprofen, meclofenamate,mefenamic acid, meloxicam, nabumetone, naproxen, oxaprozin,phenylbutazone, piroxicam, sulindac, tenoxicam, tiaprofenic acid, andtolmetin.), as well as antihistamines, aminoarylcarboxylic acidderivatives, arylacetic acid derivatives, arylbutyric acid derivatives,arylcarboxylic acids, arylpropionic acid derivatives, pyrazoles,pyrazolones, salicylic acid derivatives, thiazinecarboxamides,e-acetamidocaproic acid, S-adenosylmethionine, 3-amino-4-hydroxybutyricacid, amixetrine, bendazac, benzydamine, bucolome, difenpiramide,ditazol, emorfazone, guaiazulene, nabumetone, nimesulide, orgotein,oxaceprol, paranyline, perisoxal, pifoxime, proquazone, proxazole, andtenidap.

In an additional embodiment, the compositions of the invention areadministered alone or in combination with an anti-angiogenic agent.Anti-angiogenic agents that may be administered with the compositions ofthe invention include, but are not limited to, Angiostatin (Entremed,Rockville, Md.), Troponin-1 (Boston Life Sciences, Boston, Mass.),anti-Invasive Factor, retinoic acid and derivatives thereof, paclitaxel(Taxol), Suramin, Tissue Inhibitor of Metalloproteinase-1, TissueInhibitor of Metalloproteinase-2, VEGI, Plasminogen ActivatorInhibitor-1, Plasminogen Activator Inhibitor-2, and various forms of thelighter “d group” transition metals.

Lighter “d group” transition metals include, for example, vanadium,molybdenum, tungsten, titanium, niobium, and tantalum species. Suchtransition metal species may form transition metal complexes. Suitablecomplexes of the above-mentioned transition metal species include oxotransition metal complexes.

Representative examples of vanadium complexes include oxo vanadiumcomplexes such as vanadate and vanadyl complexes. Suitable vanadatecomplexes include metavanadate and orthovanadate complexes such as, forexample, ammonium metavanadate, sodium metavanadate, and sodiumorthovanadate. Suitable vanadyl complexes include, for example, vanadylacetylacetonate and vanadyl sulfate including vanadyl sulfate hydratessuch as vanadyl sulfate mono- and trihydrates.

Representative examples of tungsten and molybdenum complexes alsoinclude oxo complexes. Suitable oxo tungsten complexes include tungstateand tungsten oxide complexes. Suitable tungstate complexes includeammonium tungstate, calcium tungstate, sodium tungstate dihydrate, andtungstic acid. Suitable tungsten oxides include tungsten (IV) oxide andtungsten (VI) oxide. Suitable oxo molybdenum complexes includemolybdate, molybdenum oxide, and molybdenyl complexes. Suitablemolybdate complexes include ammonium molybdate and its hydrates, sodiummolybdate and its hydrates, and potassium molybdate and its hydrates.Suitable molybdenum oxides include molybdenum (VI) oxide, molybdenum(VI) oxide, and molybdic acid. Suitable molybdenyl complexes include,for example, molybdenyl acetylacetonate. Other suitable tungsten andmolybdenum complexes include hydroxo derivatives derived from, forexample, glycerol, tartaric acid, and sugars.

A wide variety of other anti-angiogenic factors may also be utilizedwithin the context of the present invention. Representative examplesinclude, but are not limited to, platelet factor 4; protamine sulphate;sulphated chitin derivatives (prepared from queen crab shells), (Murataet al., Cancer Res. 51:22-26, (1991)); Sulphated PolysaccharidePeptidoglycan Complex (SP-PG) (the function of this compound may beenhanced by the presence of steroids such as estrogen, and tamoxifencitrate); Staurosporine; modulators of matrix metabolism, including forexample, proline analogs, cishydroxyproline, d,L-3,4-dehydroproline,Thiaproline, alpha,alpha-dipyridyl, aminopropionitrile fumarate;4-propyl-5-(4-pyridinyl)-2(3H)-oxazolone; Methotrexate; Mitoxantrone;Heparin; Interferons; 2 Macroglobulin-serum; ChIMP-3 (Pavloff et al., J.Bio. Chem. 267:17321-17326, (1992)); Chymostatin (Tomkinson et al.,Biochem J. 286:475-480, (1992)); Cyclodextrin Tetradecasulfate;Eponemycin; Camptothecin; Fumagillin (Ingber et al., Nature 348:555-557,(1990)); Gold Sodium Thiomalate (“GST”; Matsubara and Ziff, J. Clin.Invest. 79:1440-1446, (1987)); anticollagenase-serum; alpha2-antiplasmin(Holmes et al., J. Biol. Chem. 262(4):1659-1664, (1987)); Bisantrene(National Cancer Institute); Lobenzarit disodium(N-(2)-carboxyphenyl-4-chloroanthronilic acid disodium or “CCA”;(Takeuchi et al., Agents Actions 36:312-316, (1992)); andmetalloproteinase inhibitors such as BB94.

Additional anti-angiogenic factors that may also be utilized within thecontext of the present invention include Thalidomide, (Celgene, Warren,N.J.); Angiostatic steroid; AGM-1470 (H. Brem and J. Folkman J Pediatr.Surg. 28:445-51 (1993)); an integrin alpha v beta 3 antagonist (C.Storgard et al., J Clin. Invest. 103:47-54 (1999));carboxynaminolmidazole; Carboxyamidotriazole (CAI) (National CancerInstitute, Bethesda, Md.); Conbretastatin A-4 (CA4P) (OXiGENE, Boston,Mass.); Squalamine (Magainin Pharmaceuticals, Plymouth Meeting, Pa.);TNP-470, (Tap Pharmaceuticals, Deerfield, Ill.); ZD-0101 AstraZeneca(London, UK); APRA (CT2584); Benefin, Byrostatin-1 (SC339555); CGP-41251(PKC 412); CM101; Dexrazoxane (ICRF187); DMXAA; Endostatin;Flavopridiol; Genestein; GTE; ImmTher; Iressa (ZD1839); Octreotide(Somatostatin); Panretin; Penacillamine; Photopoint; PI-88; Prinomastat(AG-3340) Purlytin; Suradista (FCE26644); Tamoxifen (Nolvadex);Tazarotene; Tetrathiomolybdate; Xeloda (Capecitabine); and5-Fluorouracil.

Anti-angiogenic agents that may be administered in combination with thecompounds of the invention may work through a variety of mechanismsincluding, but not limited to, inhibiting proteolysis of theextracellular matrix, blocking the function of endothelialcell-extracellular matrix adhesion molecules, by antagonizing thefunction of angiogenesis inducers such as growth factors, and inhibitingintegrin receptors expressed on proliferating endothelial cells.Examples of anti-angiogenic inhibitors that interfere with extracellularmatrix proteolysis and which may be administered in combination with thecompositions of the invention include, but are not limited to, AG-3340(Agouron, La Jolla, Calif.), BAY-12-9566 (Bayer, West Haven, Conn.),BMS-275291 (Bristol Myers Squibb, Princeton, N.J.), CGS-27032A(Novartis, East Hanover, N.J.), Marimastat (British Biotech, Oxford,UK), and Metastat (Aeterna, St-Foy, Quebec). Examples of anti-angiogenicinhibitors that act by blocking the function of endothelialcell-extracellular matrix adhesion molecules and which may beadministered in combination with the compositions of the inventioninclude, but are not limited to, EMD-121974 (Merck KcgaA Darmstadt,Germany) and Vitaxin (Ixsys, La Jolla, Calif./Medimmune, Gaithersburg,Md.). Examples of anti-angiogenic agents that act by directlyantagonizing or inhibiting angiogenesis inducers and which may beadministered in combination with the compositions of the inventioninclude, but are not limited to, Angiozyme (Ribozyme, Boulder, Colo.),Anti-VEGF antibody (Genentech, S. San Francisco, Calif.),PTK-787/ZK-225846 (Novartis, Basel, Switzerland), SU-101 (Sugen, S. SanFrancisco, Calif.), SU-5416 (Sugen/Pharmacia Upjohn, Bridgewater, N.J.),and SU-6668 (Sugen). Other anti-angiogenic agents act to indirectlyinhibit angiogenesis. Examples of indirect inhibitors of angiogenesiswhich may be administered in combination with the compositions of theinvention include, but are not limited to, IM-862 (Cytran, Kirkland,Wash.), Interferon-alpha, IL-12 (Roche, Nutley, N.J.), and Pentosanpolysulfate (Georgetown University, Washington, D.C.).

In particular embodiments, the use of compositions of the invention incombination with anti-angiogenic agents is contemplated for thetreatment, prevention, and/or amelioration of an autoimmune disease,such as for example, an autoimmune disease described herein.

In a particular embodiment, the use of compositions of the invention incombination with anti-angiogenic agents is contemplated for thetreatment, prevention, and/or amelioration of arthritis. In a moreparticular embodiment, the use of compositions of the invention incombination with anti-angiogenic agents is contemplated for thetreatment, prevention, and/or amelioration of rheumatoid arthritis.

In another embodiment, the polynucleotides encoding a polypeptide of thepresent invention are administered in combination with an angiogenicprotein, or polynucleotides encoding an angiogenic protein. Examples ofangiogenic proteins that may be administered with the compositions ofthe invention include, but are not limited to, acidic and basicfibroblast growth factors, VEGF-1, VEGF-2, VEGF-3, epidermal growthfactor alpha and beta, platelet-derived endothelial cell growth factor,platelet-derived growth factor, tumor necrosis factor alpha, hepatocytegrowth factor, insulin-like growth factor, colony stimulating factor,macrophage colony stimulating factor, granulocyte/macrophage colonystimulating factor, and nitric oxide synthase.

In additional embodiments, compositions of the invention areadministered in combination with a chemotherapeutic agent.Chemotherapeutic agents that may be administered with the albumin fusionproteins and/or polynucleotides of the invention include, but are notlimited to alkylating agents such as nitrogen mustards (for example,Mechlorethamine, cyclophosphamide, Cyclophosphamide Ifosfamide,Melphalan (L-sarcolysin), and Chlorambucil), ethylenimines andmethylmelamines (for example, Hexamethylmelamine and Thiotepa), alkylsulfonates (for example, Busulfan), nitrosoureas (for example,Carmustine (BCNU), Lomustine (CCNU), Semustine (methyl-CCNU), andStreptozocin (streptozotocin)), triazenes (for example, Dacarbazine(DTIC; dimethyltriazenoimidazolecarboxamide)), folic acid analogs (forexample, Methotrexate (amethopterin)), pyrimidine analogs (for example,Fluorouacil (5-fluorouracil; 5-FU), Floxuridine (fluorodeoxyuridine;FudR), and Cytarabine (cytosine arabinoside)), purine analogs andrelated inhibitors (for example, Mercaptopurine (6-mercaptopurine;6-MP), Thioguanine (6-thioguanine; TG), and Pentostatin(2′-deoxycoformycin)), vinca alkaloids (for example, Vinblastine (VLB,vinblastine sulfate)) and Vincristine (vincristine sulfate)),epipodophyllotoxins (for example, Etoposide and Teniposide), antibiotics(for example, Dactinomycin (actinomycin D), Daunorubicin (daunomycin;rubidomycin), Doxorubicin, Bleomycin, Plicamycin (mithramycin), andMitomycin (mitomycin C), enzymes (for example, L-Asparaginase),biological response modifiers (for example, Interferon-alpha andinterferon-alpha-2b), platinum coordination compounds (for example,Cisplatin (cis-DDP) and Carboplatin), anthracenedione (Mitoxantrone),substituted ureas (for example, Hydroxyurea), methylhydrazinederivatives (for example, Procarbazine (N-methylhydrazine; MIH),adrenocorticosteroids (for example, Prednisone), progestins (forexample, Hydroxyprogesterone caproate, Medroxyprogesterone,Medroxyprogesterone acetate, and Megestrol acetate), estrogens (forexample, Diethylstilbestrol (DES), Diethylstilbestrol diphosphate,Estradiol, and Ethinyl estradiol), antiestrogens (for example,Tamoxifen), androgens (Testosterone proprionate, and Fluoxymesterone),antiandrogens (for example, Flutamide), gonadotropin-releasing hormoneanalogs (for example, Leuprolide), other hormones and hormone analogs(for example, methyltestosterone, estramustine, estramustine phosphatesodium, chlorotrianisene, and testolactone), and others (for example,dicarbazine, glutamic acid, and mitotane).

In one embodiment, the compositions of the invention are administered incombination with one or more of the following drugs: infliximab (alsoknown as Remicade™ Centocor, Inc.), Trocade (Roche, RO-32-3555),Leflunomide (also known as Arava™ from Hoechst Marion Roussel), Kineret™(an IL-1 Receptor antagonist also known as Anakinra from Amgen, Inc.)

In a specific embodiment, compositions of the invention are administeredin combination with CHOP (cyclophosphamide, doxorubicin, vincristine,and prednisone) or combination of one or more of the components of CHOP.In one embodiment, the compositions of the invention are administered incombination with anti-CD20 antibodies, human monoclonal anti-CD20antibodies. In another embodiment, the compositions of the invention areadministered in combination with anti-CD20 antibodies and CHOP, oranti-CD20 antibodies and any combination of one or more of thecomponents of CHOP, particularly cyclophosphamide and/or prednisone. Ina specific embodiment, compositions of the invention are administered incombination with Rituximab. In a further embodiment, compositions of theinvention are administered with Rituximab and CHOP, or Rituximab and anycombination of one or more of the components of CHOP, particularlycyclophosphamide and/or prednisone. In a specific embodiment,compositions of the invention are administered in combination withtositumomab. In a further embodiment, compositions of the invention areadministered with tositumomab and CHOP, or tositumomab and anycombination of one or more of the components of CHOP, particularlycyclophosphamide and/or prednisone. The anti-CD20 antibodies mayoptionally be associated with radioisotopes, toxins or cytotoxicprodrugs.

In another specific embodiment, the compositions of the invention areadministered in combination Zevalin™. In a further embodiment,compositions of the invention are administered with Zevalin™ and CHOP,or Zevalin™ and any combination of one or more of the components ofCHOP, particularly cyclophosphamide and/or prednisone. Zevalin™ may beassociated with one or more radioisotopes. Particularly preferredisotopes are ⁹⁰Y and ¹¹¹In.

In an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withcytokines. Cytokines that may be administered with the albumin fusionproteins and/or polynucleotides of the invention include, but are notlimited to, IL2, IL3, IL4, IL5, IL6, IL7, IL10, IL12, IL13, IL15,anti-CD40, CD40L, IFN-gamma and TNF-alpha. In another embodiment,albumin fusion proteins and/or polynucleotides of the invention may beadministered with any interleukin, including, but not limited to, IL-1alpha, IL-1beta, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10,IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20,and IL-21.

In one embodiment, the albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with members of the TNFfamily. TNF, TNF-related or TNF-like molecules that may be administeredwith the albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, soluble forms of TNF-alpha,lymphotoxin-alpha (LT-alpha, also known as TNF-beta), LT-beta (found incomplex heterotrimer LT-alpha2-beta), OPGL, FasL, CD27L, CD30L, CD40L,4-1BBL, DcR3, OX40L, TNF-gamma (International Publication No. WO96/14328), AIM-I (International Publication No. WO 97/33899),endokine-alpha (International Publication No. WO 98/07880), OPG, andneutrokine-alpha (International Publication No. WO 98/18921, OX40, andnerve growth factor (NGF), and soluble forms of Fas, CD30, CD27, CD40and 4-IBB, TR2 (International Publication No. WO 96/34095), DR3(International Publication No. WO 97/33904), DR4 (InternationalPublication No. WO 98/32856), TR5 (International Publication No. WO98/30693), TRANK, TR9 (International Publication No. WO 98/56892), TR10(International Publication No. WO 98/54202), 312C2 (InternationalPublication No. WO 98/06842), and TR12, and soluble forms CD154, CD70,and CD153.

In an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withangiogenic proteins. Angiogenic proteins that may be administered withthe albumin fusion proteins and/or polynucleotides of the inventioninclude, but are not limited to, Glioma Derived Growth Factor (GDGF), asdisclosed in European Patent Number EP-399816; Platelet Derived GrowthFactor-A (PDGF-A), as disclosed in European Patent Number EP-682110;Platelet Derived Growth Factor-B (PDGF-B), as disclosed in EuropeanPatent Number EP-282317; Placental Growth Factor (PlGF), as disclosed inInternational Publication Number WO 92/06194; Placental Growth Factor-2(PlGF-2), as disclosed in Hauser et al., Growth Factors, 4:259-268(1993); Vascular Endothelial Growth Factor (VEGF), as disclosed inInternational Publication Number WO 90/13649; Vascular EndothelialGrowth Factor-A (VEGF-A), as disclosed in European Patent NumberEP-506477; Vascular Endothelial Growth Factor-2 (VEGF-2), as disclosedin International Publication Number WO 96/39515; Vascular EndothelialGrowth Factor B (VEGF-3); Vascular Endothelial Growth Factor B-186(VEGF-B186), as disclosed in International Publication Number WO96/26736; Vascular Endothelial Growth Factor-D (VEGF-D), as disclosed inInternational Publication Number WO 98/02543; Vascular EndothelialGrowth Factor-D (VEGF-D), as disclosed in International PublicationNumber WO 98/07832; and Vascular Endothelial Growth Factor-E (VEGF-E),as disclosed in German Patent Number DE19639601. The above mentionedreferences are herein incorporated by reference in their entireties.

In an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withFibroblast Growth Factors. Fibroblast Growth Factors that may beadministered with the albumin fusion proteins and/or polynucleotides ofthe invention include, but are not limited to, FGF-1, FGF-2, FGF-3,FGF-4, FGF-5, FGF-6, FGF-7, FGF-8, FGF-9, FGF-10, FGF-11, FGF-12,FGF-13, FGF-14, and FGF-15.

In an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withhematopoietic growth factors. Hematopoietic growth factors that may beadministered with the albumin fusion proteins and/or polynucleotides ofthe invention include, but are not limited to, granulocyte macrophagecolony stimulating factor (GM-CSF) (sargramostim, LEUKINE™ PROKINE™),granulocyte colony stimulating factor (G-CSF) (filgrastim, NEUPOGEN™)macrophage colony stimulating factor (M-CSF, CSF-1) erythropoietin(epoetin alfa, EPOGEN™, PROCRIT™), stem cell factor (SCF, c-kit ligand,steel factor), megakaryocyte colony stimulating factor, PIXY321 (aGMCSF/IL-3 fusion protein), interleukins, especially any one or more ofIL-1 through IL-12, interferon-gamma, or thrombopoietin.

In certain embodiments, albumin fusion proteins and/or polynucleotidesof the present invention are administered in combination with adrenergicblockers, such as, for example, acebutolol, atenolol, betaxolol,bisoprolol, carteolol, labetalol, metoprolol, nadolol, oxprenolol,penbutolol, pindolol, propranolol, sotalol, and timolol.

In another embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination with anantiarrhythmic drug (e.g., adenosine, amidoarone, bretylium, digitalis,digoxin, digitoxin, diliazem, disopyramide, esmolol, flecainide,lidocaine, mexiletine, moricizine, phenytoin, procainamide, N-acetylprocainamide, propafenone, propranolol, quinidine, sotalol, tocainide,and verapamil).

In another embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withdiuretic agents, such as carbonic anhydrase-inhibiting agents (e.g.,acetazolamide, dichlorphenamide, and methazolamide), osmotic diuretics(e.g., glycerin, isosorbide, mannitol, and urea), diuretics that inhibitNat K⁺-2Cl⁻ symport (e.g., furosemide, bumetanide, azosemide,piretanide, tripamide, ethacrynic acid, muzolimine, and torsemide),thiazide and thiazide-like diuretics (e.g., bendroflumethiazide,benzthiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide,methyclothiazide, polythiazide, trichormethiazide, chlorthalidone,indapamide, metolazone, and quinethazone), potassium sparing diuretics(e.g., amiloride and triamterene), and mineralcorticoid receptorantagonists (e.g., spironolactone, canrenone, and potassium canrenoate).

In one embodiment, the albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with treatments forendocrine and/or hormone imbalance disorders. Treatments for endocrineand/or hormone imbalance disorders include, but are not limited to,¹²⁷I, radioactive isotopes of iodine such as ¹³¹I and ¹²³I; recombinantgrowth hormone, such as HUMATROPE™ (recombinant somatropin); growthhormone analogs such as PROTROPIN™ (somatrem); dopamine agonists such asPARLODEL™ (bromocriptine); somatostatin analogs such as SANDOSTATIN™(octreotide); gonadotropin preparations such as PREGNYL™, A.P.L.™ andPROFASI™ (chorionic gonadotropin (CG)), PERGONAL™ (menotropins), andMETRODIN™ (urofollitropin (uFSH)); synthetic human gonadotropinreleasing hormone preparations such as FACTREL™ and LUTREPULSE™(gonadorelin hydrochloride); synthetic gonadotropin agonists such asLUPRON™ (leuprolide acetate), SUPPRELIN™ (histrelin acetate), SYNAREL™(nafarelin acetate), and ZOLADEX™ (goserelin acetate); syntheticpreparations of thyrotropin-releasing hormone such as RELEFACT TRH™ andTHYPINONE™ (protirelin); recombinant human TSH such as THYROGEN™;synthetic preparations of the sodium salts of the natural isomers ofthyroid hormones such as L-T₄™, SYNTHROID™ and LEVOTHROID™(levothyroxine sodium), L-T₃™, CYTOMEL™ and TRIOSTAT™ (liothyroinesodium), and THYROLAR™ (liotrix); antithyroid compounds such as6-n-propylthiouracil (propylthiouracil), 1-methyl-2-mercaptoimidazoleand TAPAZOLE™ (methimazole), NEO-MERCAZOLE™ (carbimazole);beta-adrenergic receptor antagonists such as propranolol and esmolol;Ca²⁺ channel blockers; dexamethasone and iodinated radiological contrastagents such as TELEPAQUE™ (iopanoic acid) and ORAGRAFIN™ (sodiumipodate).

Additional treatments for endocrine and/or hormone imbalance disordersinclude, but are not limited to, estrogens or conjugated estrogens suchas ESTRACE™ (estradiol), ESTINYL™ (ethinyl estradiol), PREMARIN™,ESTRATAB™, ORTHO-EST™, OGEN™ and estropipate (estrone), ESTROVIS™(quinestrol), ESTRADERM™ (estradiol), DELESTROGEN™ and VALERGEN™(estradiol valerate), DEPO-ESTRADIOL CYPIONATE™ and ESTROJECT LA™(estradiol cypionate); antiestrogens such as NOLVADEX™ (tamoxifen),SEROPHENE™ and CLOMID™ (clomiphene); progestins such as DURALUTIN™(hydroxyprogesterone caproate), MPA™ and DEPO-PROVERA™(medroxyprogesterone acetate), PROVERA™ and CYCRIN™ (MPA), MEGACE™(megestrol acetate), NORLUTIN™ (norethindrone), and NORLUTATE™ andAYGESTIN™ (norethindrone acetate); progesterone implants such asNORPLANT SYSTEM™ (subdermal implants of norgestrel); antiprogestins suchas RU 486™ (mifepristone); hormonal contraceptives such as ENOVID™(norethynodrel plus mestranol), PROGESTASERT™ (intrauterine device thatreleases progesterone), LOESTRIN™, BREVICON™, MODICON™ GENORA™, NELONA™,NORINYL™, OVACON-35™ and OVACON-50™ (ethinyl estradiol/norethindrone),LEVLEN™, NORDETTE™, TRI-LEVLEN™ and TRIPHASIL-21™ (ethinylestradiol/levonorgestrel) LO/OVRAL™ and OVRAL™ (ethinylestradiol/norgestrel), DEMULEN™ (ethinyl estradiol/ethynodioldiacetate), NORINYL™ ORTHO-NOVUM™, NORETHIN™, GENORA™, and NELOVA™(norethindrone/mestranol), DESOGEN™ and ORTHO-CEPT™ (ethinylestradiol/desogestrel), ORTHO-CYCLEN™ and ORTHO-TRICYCLEN™ (ethinylestradiol/norgestimate), MICRONOR™ and NOR-QD™ (norethindrone), andOVRETTE™ (norgestrel).

Additional treatments for endocrine and/or hormone imbalance disordersinclude, but are not limited to, testosterone esters such as methenoloneacetate and testosterone undecanoate; parenteral and oral androgens suchas TESTOJECT-50™ (testosterone), TESTEX™ (testosterone propionate),DELATESTRYL™ (testosterone enanthate), DEPO-TESTOSTERONE™ (testosteronecypionate), DANOCRINE™ (danazol), HALOTESTIN™ (fluoxymesterone), ORETONMETHYL™, TESTRED™ and VIRILON™ (methyltestosterone), and OXANDRIN™(oxandrolone); testosterone transdermal systems such as TESTODERM™;androgen receptor antagonist and 5-alpha-reductase inhibitors such asANDROCUR™ (cyproterone acetate), EULEXIN™ (flutamide), and PROSCAR™(finasteride); adrenocorticotropic hormone preparations such asCORTROSYN™ (cosyntropin); adrenocortical steroids and their syntheticanalogs such as ACLOVATE™ (alclometasone dipropionate), CYCLOCORT™(amcinonide), BECLOVENT™ and VANCERIL™ (beclomethasone dipropionate),CELESTONE™ (betamethasone), BENISONE™ and UTICORT™ (betamethasonebenzoate), DIPROSONE™ (betamethasone dipropionate), CELESTONE PHOSPHATE™(betamethasone sodium phosphate), CELESTONE SOLUSPAN™ (betamethasonesodium phosphate and acetate), BETA-VAL™ and VALISONE™ (betamethasonevalerate), TEMOVATE™ (clobetasol propionate), CLODERM™ (clocortolonepivalate), CORTEF™ and HYDROCORTONE™ (cortisol (hydrocortisone)),HYDROCORTONE ACETATE™ (cortisol (hydrocortisone) acetate), LOCOID™(cortisol (hydrocortisone) butyrate), HYDROCORTONE PHOSPHATE™ (cortisol(hydrocortisone) sodium phosphate), A-HYDROCORT™ and SOLU CORTEF™(cortisol (hydrocortisone) sodium succinate), WESTCORT™ (cortisol(hydrocortisone) valerate), CORTISONE ACETATE™ (cortisone acetate),DESOWEN™ and TRIDESILON™ (desonide), TOPICORT™ (desoximetasone),DECADRON™ (dexamethasone), DECADRON LA™ (dexamethasone acetate),DECADRON PHOSPHATE™ and HEXADROL PHOSPHATE™ (dexamethasone sodiumphosphate), FLORONE™ and MAXIFLOR™ (diflorasone diacetate), FLORINEFACETATE™ (fludrocortisone acetate), AEROBID™ and NASALIDE™(flunisolide), FLUONID™ and SYNALAR™ (fluocinolone acetonide), LIDEX™(fluocinonide), FLUOR-OP™ and FML™ (fluorometholone), CORDRAN™(flurandrenolide), HALOG™ (halcinonide), HMS LIZUIFILM™ (medrysone),MEDROL™ (methylprednisolone), DEPO-MEDROL™ and MEDROL ACETATE™(methylprednisone acetate), A-METHAPRED™ and SOLUMEDROL™(methylprednisolone sodium succinate), ELOCON™ (mometasone furoate),HALDRONE™ (paramethasone acetate), DELTA-CORTEF™ (prednisolone),ECONOPRED™ (prednisolone acetate), HYDELTRASOL™ (prednisolone sodiumphosphate), HYDELTRA-T.B.A™ (prednisolone tebutate), DELTASONE™(prednisone), ARISTOCORT™ and KENACORT™ (triamcinolone), KENALOG™(triamcinolone acetonide), ARISTOCORT™ and KENACORT DIACETATE™(triamcinolone diacetate), and ARISTOSPAN™ (triamcinolone hexacetonide);inhibitors of biosynthesis and action of adrenocortical steroids such asCYTADREN™ (aminoglutethimide), NIZORAL™ (ketoconazole), MODRASTANE™(trilostane), and METOPIRONE™ (metyrapone); bovine, porcine or humaninsulin or mixtures thereof; insulin analogs; recombinant human insulinsuch as HUMULIN™ and NOVOLIN™; oral hypoglycemic agents such asORAIVIIDE™ and ORINASE™ (tolbutamide), DIABINESE™ (chlorpropamide),TOLAMIDE™ and TOLINASE™ (tolazamide), DYMELOR™ (acetohexamide),glibenclamide, MICRONASE™, DIBETA™ and GLYNASE™ (glyburide), GLUCOTROL™(glipizide), and DIAMICRON™ (gliclazide), GLUCOPHAGE™ (metformin),ciglitazone, pioglitazone, and alpha-glucosidase inhibitors; bovine orporcine glucagon; somatostatins such as SANDOSTATIN™ (octreotide); anddiazoxides such as PROGLYCEM™ (diazoxide).

In one embodiment, the albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with treatments foruterine motility disorders. Treatments for uterine motility disordersinclude, but are not limited to, estrogen drugs such as conjugatedestrogens (e.g., PREMARIN® and ESTRATAB®), estradiols (e.g., CLIMARA®and ALORA®), estropipate, and chlorotrianisene; progestin drugs (e.g.,AMEN® (medroxyprogesterone), MICRONOR® (norethindrone acetate),PROMETRIUM® progesterone, and megestrol acetate); andestrogen/progesterone combination therapies such as, for example,conjugated estrogens/medroxyprogesterone (e.g., PREMPRO™ and PREMPHASE®)and norethindrone acetate/ethinyl estsradiol (e.g., FEMHRT™).

In an additional embodiment, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withdrugs effective in treating iron deficiency and hypochromic anemias,including but not limited to, ferrous sulfate (iron sulfate, FEOSOL™),ferrous fumarate (e.g., FEOSTAT™), ferrous gluconate (e.g., FERGON™),polysaccharide-iron complex (e.g., NIFEREX™), iron dextran injection(e.g., INFED™), cupric sulfate, pyroxidine, riboflavin, Vitamin B₁₂,cyancobalamin injection (e.g., REDISOL™, RUBRAMIN PC™),hydroxocobalamin, folic acid (e.g., FOLVITE™), leucovorin (folinic acid,5-CHOH4PteGlu, citrovorum factor) or WELLCOVORIN (Calcium salt ofleucovorin), transferrin or ferritin.

In certain embodiments, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withagents used to treat psychiatric disorders. Psychiatric drugs that maybe administered with the albumin fusion proteins and/or polynucleotidesof the invention include, but are not limited to, antipsychotic agents(e.g., chlorpromazine, chlorprothixene, clozapine, fluphenazine,haloperidol, loxapine, mesoridazine, molindone, olanzapine,perphenazine, pimozide, quetiapine, risperidone, thioridazine,thiothixene, trifluoperazine, and triflupromazine), antimanic agents(e.g., carbamazepine, divalproex sodium, lithium carbonate, and lithiumcitrate), antidepressants (e.g., amitriptyline, amoxapine, bupropion,citalopram, clomipramine, desipramine, doxepin, fluvoxamine, fluoxetine,imipramine, isocarboxazid, maprotiline, mirtazapine, nefazodone,nortriptyline, paroxetine, phenelzine, protriptyline, sertraline,tranylcypromine, trazodone, trimipramine, and venlafaxine), antianxietyagents (e.g., alprazolam, buspirone, chlordiazepoxide, clorazepate,diazepam, halazepam, lorazepam, oxazepam, and prazepam), and stimulants(e.g., d-amphetamine, methylphenidate, and pemoline).

In other embodiments, the albumin fusion proteins and/or polynucleotidesof the invention are administered in combination with agents used totreat neurological disorders. Neurological agents that may beadministered with the albumin fusion proteins and/or polynucleotides ofthe invention include, but are not limited to, antiepileptic agents(e.g., carbamazepine, clonazepam, ethosuximide, phenobarbital,phenytoin, primidone, valproic acid, divalproex sodium, felbamate,gabapentin, lamotrigine, levetiracetam, oxcarbazepine, tiagabine,topiramate, zonisamide, diazepam, lorazepam, and clonazepam),antiparkinsonian agents (e.g., levodopa/carbidopa, selegiline,amantidine, bromocriptine, pergolide, ropinirole, pramipexole,benztropine; biperiden; ethopropazine; procyclidine; trihexyphenidyl,tolcapone), and ALS therapeutics (e.g. riluzole).

In another embodiment, albumin fusion proteins and/or polynucleotides ofthe invention are administered in combination with vasodilating agentsand/or calcium channel blocking agents. Vasodilating agents that may beadministered with the albumin fusion proteins and/or polynucleotides ofthe invention include, but are not limited to, Angiotensin ConvertingEnzyme (ACE) inhibitors (e.g., papaverine, isoxsuprine, benazepril,captopril, cilazapril, enalapril, enalaprilat, fosinopril, lisinopril,moexipril, perindopril, quinapril, ramipril, spirapril, trandolapril,and nylidrin), and nitrates (e.g., isosorbide dinitrate, isosorbidemononitrate, and nitroglycerin). Examples of calcium channel blockingagents that may be administered in combination with the albumin fusionproteins and/or polynucleotides of the invention include, but are notlimited to amlodipine, bepridil, diltiazem, felodipine, flunarizine,isradipine, nicardipine, nifedipine, nimodipine, and verapamil.

In certain embodiments, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withtreatments for gastrointestinal disorders. Treatments forgastrointestinal disorders that may be administered with the albuminfusion protein and/or polynucleotide of the invention include, but arenot limited to, H₂ histamine receptor antagonists (e.g., TAGAMET™(cimetidine), ZANTAC™ (ranitidine), PEPCID™ (famotidine), and AXID™(nizatidine)); inhibitors of H⁺, K⁺ ATPase (e.g.,PREVACID™(lansoprazole) and PRILOSEC™ (omeprazole)); Bismuth compounds(e.g., PEPTO-BISMOL™ (bismuth subsalicylate) and DE-NOL™ (bismuthsubcitrate)); various antacids; sucralfate; prostaglandin analogs (e.g.CYTOTEC™ (misoprostol)); muscarinic cholinergic antagonists; laxatives(e.g., surfactant laxatives, stimulant laxatives, saline and osmoticlaxatives); antidiarrheal agents (e.g., LOMOTIL™ (diphenoxylate),MOTOFEN™ (diphenoxin), and IMODIUM™ (loperamide hydrochloride)),synthetic analogs of somatostatin such as SANDOSTATIN™ (octreotide),antiemetic agents (e.g., ZOFRAN™ (ondansetron), KYTRIL™ (granisetronhydrochloride), tropisetron, dolasetron, metoclopramide, chlorpromazine,perphenazine, prochlorperazine, promethazine, thiethylperazine,triflupromazine, domperidone, haloperidol, droperidol,trimethobenzamide, dexamethasone, methylprednisolone, dronabinol, andnabilone); D2 antagonists (e.g., metoclopramide, trimethobenzamide andchlorpromazine); bile salts; chenodeoxycholic acid; ursodeoxycholicacid; and pancreatic enzyme preparations such as pancreatin andpancrelipase.

In additional embodiments, the albumin fusion proteins and/orpolynucleotides of the invention are administered in combination withother therapeutic or prophylactic regimens, such as, for example,radiation therapy.

The invention also provides a pharmaceutical pack or kit comprising oneor more containers filled with one or more of the ingredients of thepharmaceutical compositions comprising albumin fusion proteins of theinvention. Optionally associated with such container(s) can be a noticein the form prescribed by a governmental agency regulating themanufacture, use or sale of pharmaceuticals or biological products,which notice reflects approval by the agency of manufacture, use or salefor human administration.

Gene Therapy

Constructs encoding albumin fusion proteins of the invention can be usedas a part of a gene therapy protocol to deliver therapeuticallyeffective doses of the albumin fusion protein. A preferred approach forin vivo introduction of nucleic acid into a cell is by use of a viralvector containing nucleic acid, encoding an albumin fusion protein ofthe invention. Infection of cells with a viral vector has the advantagethat a large proportion of the targeted cells can receive the nucleicacid. Additionally, molecules encoded within the viral vector, e.g., bya cDNA contained in the viral vector, are expressed efficiently in cellswhich have taken up viral vector nucleic acid.

Retrovirus vectors and adeno-associated virus vectors can be used as arecombinant gene delivery system for the transfer of exogenous nucleicacid molecules encoding albumin fusion proteins in vivo. These vectorsprovide efficient delivery of nucleic acids into cells, and thetransferred nucleic acids are stably integrated into the chromosomal DNAof the host. The development of specialized cell lines (termed“packaging cells”) which produce only replication-defective retroviruseshas increased the utility of retroviruses for gene therapy, anddefective retroviruses are characterized for use in gene transfer forgene therapy purposes (for a review see Miller, A. D. (1990) Blood 76:271). A replication defective retrovirus can be packaged into virionswhich can be used to infect a target cell through the use of a helpervirus by standard techniques. Protocols for producing recombinantretroviruses and for infecting cells in vitro or in vivo with suchviruses can be found in Current Protocols in Molecular Biology, Ausubel,F. M. et al., (eds.) Greene Publishing Associates, (1989), Sections9.10-9.14 and other standard laboratory manuals.

Another viral gene delivery system useful in the present invention usesadenovirus-derived vectors. The genome of an adenovirus can bemanipulated such that it encodes and expresses a gene product ofinterest but is inactivated in terms of its ability to replicate in anormal lytic viral life cycle. See, for example, Berkner et al.,BioTechniques 6:616 (1988); Rosenfeld et al., Science 252:431-434(1991); and Rosenfeld et al., Cell 68:143-155 (1992). Suitableadenoviral vectors derived from the adenovirus strain Ad type 5 d1324 orother strains of adenovirus (e.g., Ad2, Ad3, Ad7 etc.) are known tothose skilled in the art. Recombinant adenoviruses can be advantageousin certain circumstances in that they are not capable of infectingnondividing cells and can be used to infect a wide variety of celltypes, including epithelial cells (Rosenfeld et al., (1992) citedsupra). Furthermore, the virus particle is relatively stable andamenable to purification and concentration, and as above, can bemodified so as to affect the spectrum of infectivity. Additionally,introduced adenoviral DNA (and foreign DNA contained therein) is notintegrated into the genome of a host cell but remains episomal, therebyavoiding potential problems that can occur as a result of insertionalmutagenesis in situations where introduced DNA becomes integrated intothe host genome (e.g., retroviral DNA). Moreover, the carrying capacityof the adenoviral genome for foreign DNA is large (up to 8 kilobases)relative to other gene delivery vectors (Berkner et al., cited supra;Haj-Ahmand et al., J. Virol. 57:267 (1986)).

In another embodiment, non-viral gene delivery systems of the presentinvention rely on endocytic pathways for the uptake of the subjectnucleotide molecule by the targeted cell. Exemplary gene deliverysystems of this type include liposomal derived systems, poly-lysineconjugates, and artificial viral envelopes. In a representativeembodiment, a nucleic acid molecule encoding an albumin fusion proteinof the invention can be entrapped in liposomes bearing positive chargeson their surface (e.g., lipofectins) and (optionally) which are taggedwith antibodies against cell surface antigens of the target tissue(Mizuno et al. (1992) No Shinkei Geka 20:547-5 5 1; PCT publicationWO91/06309; Japanese patent application 1047381; and European patentpublication EP-A-43075).

Gene delivery systems for a gene encoding an albumin fusion protein ofthe invention can be introduced into a patient by any of a number ofmethods. For instance, a pharmaceutical preparation of the gene deliverysystem can be introduced systemically, e.g. by intravenous injection,and specific transduction of the protein in the target cells occurspredominantly from specificity of transfection provided by the genedelivery vehicle, cell-type or tissue-type expression due to thetranscriptional regulatory sequences controlling expression of thereceptor gene, or a combination thereof. In other embodiments, initialdelivery of the recombinant gene is more limited with introduction intothe animal being quite localized. For example, the gene delivery vehiclecan be introduced by catheter (see U.S. Pat. No. 5,328,470) or byStereotactic injection (e.g. Chen et al. (1994) PNAS 91: 3 054-3 05 7).The pharmaceutical preparation of the gene therapy construct can consistessentially of the gene delivery system in an acceptable diluent, or cancomprise a slow release matrix in which the gene delivery vehicle isimbedded. Where the albumin fusion protein can be produced intact fromrecombinant cells, e.g. retroviral vectors, the pharmaceuticalpreparation can comprise one or more cells which produce the albuminfusion protein.

Additional Gene Therapy Methods

Also encompassed by the invention are gene therapy methods for treatingor preventing disorders, diseases and conditions. The gene therapymethods relate to the introduction of nucleic acid (DNA, RNA andantisense DNA or RNA) sequences into an animal to achieve expression ofan albumin fusion protein of the invention. This method requires apolynucleotide which codes for an albumin fusion protein of the presentinvention operatively linked to a promoter and any other geneticelements necessary for the expression of the fusion protein by thetarget tissue. Such gene therapy and delivery techniques are known inthe art, see, for example, WO90/11092, which is herein incorporated byreference.

Thus, for example, cells from a patient may be engineered with apolynucleotide (DNA or RNA) comprising a promoter operably linked to apolynucleotide encoding an albumin fusion protein of the presentinvention ex vivo, with the engineered cells then being provided to apatient to be treated with the fusion protein of the present invention.Such methods are well-known in the art. For example, see Belldegrun, A.,et al., J. Natl. Cancer Inst. 85: 207-216 (1993); Ferrantini, M. et al.,Cancer Research 53: 1107-1112 (1993); Ferrantini, M. et al., J.Immunology 153: 4604-4615 (1994); Kaido, T., et al., Int. J. Cancer 60:221-229 (1995); Ogura, H., et al., Cancer Research 50: 5102-5106 (1990);Santodonato, L., et al., Human Gene Therapy 7:1-10 (1996); Santodonato,L., et al., Gene Therapy 4:1246-1255 (1997); and Zhang, J.-F. et al.,Cancer Gene Therapy 3: 31-38 (1996)), which are herein incorporated byreference. In one embodiment, the cells which are engineered arearterial cells. The arterial cells may be reintroduced into the patientthrough direct injection to the artery, the tissues surrounding theartery, or through catheter injection.

As discussed in more detail below, the polynucleotide constructs can bedelivered by any method that delivers injectable materials to the cellsof an animal, such as, injection into the interstitial space of tissues(heart, muscle, skin, lung, liver, and the like). The polynucleotideconstructs may be delivered in a pharmaceutically acceptable liquid oraqueous carrier.

In one embodiment, polynucleotides encoding the albumin fusion proteinsof the present invention is delivered as a naked polynucleotide. Theterm “naked” polynucleotide, DNA or RNA refers to sequences that arefree from any delivery vehicle that acts to assist, promote orfacilitate entry into the cell, including viral sequences, viralparticles, liposome formulations, lipofectin or precipitating agents andthe like. However, polynucleotides encoding the albumin fusion proteinsof the present invention can also be delivered in liposome formulationsand lipofectin formulations and the like can be prepared by methods wellknown to those skilled in the art. Such methods are described, forexample, in U.S. Pat. Nos. 5,593,972, 5,589,466, and 5,580,859, whichare herein incorporated by reference.

The polynucleotide vector constructs used in the gene therapy method arepreferably constructs that will not integrate into the host genome norwill they contain sequences that allow for replication. Appropriatevectors include pWLNEO, pSV2CAT, pOG44, pXT1 and pSG available fromStratagene; pSVK3, pBPV, pMSG and pSVL available from Pharmacia; andpEF1/V5, pcDNA3.1, and pRc/CMV2 available from Invitrogen. Othersuitable vectors will be readily apparent to the skilled artisan.

Any strong promoter known to those skilled in the art can be used fordriving the expression of the polynucleotide sequence. Suitablepromoters include adenoviral promoters, such as the adenoviral majorlate promoter; or heterologous promoters, such as the cytomegalovirus(CMV) promoter; the respiratory syncytial virus (RSV) promoter;inducible promoters, such as the MMT promoter, the metallothioneinpromoter; heat shock promoters; the albumin promoter; the ApoAIpromoter; human globin promoters; viral thymidine kinase promoters, suchas the Herpes Simplex thymidine kinase promoter; retroviral LTRs; theb-actin promoter; and human growth hormone promoters. The promoter alsomay be the native promoter for the gene corresponding to the Therapeuticprotein portion of the albumin fusion proteins of the invention.

Unlike other gene therapy techniques, one major advantage of introducingnaked nucleic acid sequences into target cells is the transitory natureof the polynucleotide synthesis in the cells. Studies have shown thatnon-replicating DNA sequences can be introduced into cells to provideproduction of the desired polypeptide for periods of up to six months.

The polynucleotide construct can be delivered to the interstitial spaceof tissues within the an animal, including of muscle, skin, brain, lung,liver, spleen, bone marrow, thymus, heart, lymph, blood, bone,cartilage, pancreas, kidney, gall bladder, stomach, intestine, testis,ovary, uterus, rectum, nervous system, eye, gland, and connectivetissue. Interstitial space of the tissues comprises the intercellular,fluid, mucopolysaccharide matrix among the reticular fibers of organtissues, elastic fibers in the walls of vessels or chambers, collagenfibers of fibrous tissues, or that same matrix within connective tissueensheathing muscle cells or in the lacunae of bone. It is similarly thespace occupied by the plasma of the circulation and the lymph fluid ofthe lymphatic channels. Delivery to the interstitial space of muscletissue is preferred for the reasons discussed below. They may beconveniently delivered by injection into the tissues comprising thesecells. They are preferably delivered to and expressed in persistent,non-dividing cells which are differentiated, although delivery andexpression may be achieved in non-differentiated or less completelydifferentiated cells, such as, for example, stem cells of blood or skinfibroblasts. In vivo muscle cells are particularly competent in theirability to take up and express polynucleotides.

For the naked nucleic acid sequence injection, an effective dosageamount of DNA or RNA will be in the range of from about 0.05 mg/kg bodyweight to about 50 mg/kg body weight. Preferably the dosage will be fromabout 0.005 mg/kg to about 20 mg/kg and more preferably from about 0.05mg/kg to about 5 mg/kg. Of course, as the artisan of ordinary skill willappreciate, this dosage will vary according to the tissue site ofinjection. The appropriate and effective dosage of nucleic acid sequencecan readily be determined by those of ordinary skill in the art and maydepend on the condition being treated and the route of administration.

The preferred route of administration is by the parenteral route ofinjection into the interstitial space of tissues. However, otherparenteral routes may also be used, such as, inhalation of an aerosolformulation particularly for delivery to lungs or bronchial tissues,throat or mucous membranes of the nose. In addition, naked DNAconstructs can be delivered to arteries during angioplasty by thecatheter used in the procedure.

The naked polynucleotides are delivered by any method known in the art,including, but not limited to, direct needle injection at the deliverysite, intravenous injection, topical administration, catheter infusion,and so-called “gene guns”. These delivery methods are known in the art.

The constructs may also be delivered with delivery vehicles such asviral sequences, viral particles, liposome formulations, lipofectin,precipitating agents, etc. Such methods of delivery are known in theart.

In certain embodiments, the polynucleotide constructs are complexed in aliposome preparation. Liposomal preparations for use in the instantinvention include cationic (positively charged), anionic (negativelycharged) and neutral preparations. However, cationic liposomes areparticularly preferred because a tight charge complex can be formedbetween the cationic liposome and the polyanionic nucleic acid. Cationicliposomes have been shown to mediate intracellular delivery of plasmidDNA (Felgner et al., Proc. Natl. Acad. Sci. USA (1987) 84:7413-7416,which is herein incorporated by reference); mRNA (Malone et al., Proc.Natl. Acad. Sci. USA (1989) 86:6077-6081, which is herein incorporatedby reference); and purified transcription factors (Debs et al., J. Biol.Chem. (1990) 265:10189-10192, which is herein incorporated byreference), in functional form.

Cationic liposomes are readily available. For example,N[1-2,3-dioleyloxy)propyl]-N,N,N-triethylammonium (DOTMA) liposomes areparticularly useful and are available under the trademark Lipofectin,from GIBCO BRL, Grand Island, N.Y. (See, also, Felgner et al., Proc.Natl Acad. Sci. USA (1987) 84:7413-7416, which is herein incorporated byreference). Other commercially available liposomes include transfectace(DDAB/DOPE) and DOTAP/DOPE (Boehringer).

Other cationic liposomes can be prepared from readily availablematerials using techniques well known in the art. See, e.g. PCTPublication No. WO 90/11092 (which is herein incorporated by reference)for a description of the synthesis of DOTAP(1,2-bis(oleoyloxy)-3-(trimethylammonio)propane) liposomes. Preparationof DOTMA liposomes is explained in the literature, see, e.g., P. Felgneret al., Proc. Natl. Acad. Sci. USA 84:7413-7417, which is hereinincorporated by reference. Similar methods can be used to prepareliposomes from other cationic lipid materials.

Similarly, anionic and neutral liposomes are readily available, such asfrom Avanti Polar Lipids (Birmingham, Ala.), or can be easily preparedusing readily available materials. Such materials include phosphatidyl,choline, cholesterol, phosphatidyl ethanolamine, dioleoylphosphatidylcholine (DOPC), dioleoylphosphatidyl glycerol (DOPG),dioleoylphoshatidyl ethanolamine (DOPE), among others. These materialscan also be mixed with the DOTMA and DOTAP starting materials inappropriate ratios. Methods for making liposomes using these materialsare well known in the art.

For example, commercially dioleoylphosphatidyl choline (DOPC),dioleoylphosphatidyl glycerol (DOPG), and dioleoylphosphatidylethanolamine (DOPE) can be used in various combinations to makeconventional liposomes, with or without the addition of cholesterol.Thus, for example, DOPG/DOPC vesicles can be prepared by drying 50 mgeach of DOPG and DOPC under a stream of nitrogen gas into a sonicationvial. The sample is placed under a vacuum pump overnight and is hydratedthe following day with deionized water. The sample is then sonicated for2 hours in a capped vial, using a Heat Systems model 350 sonicatorequipped with an inverted cup (bath type) probe at the maximum settingwhile the bath is circulated at 15EC. Alternatively, negatively chargedvesicles can be prepared without sonication to produce multilamellarvesicles or by extrusion through nucleopore membranes to produceunilamellar vesicles of discrete size. Other methods are known andavailable to those of skill in the art.

The liposomes can comprise multilamellar vesicles (MLVs), smallunilamellar vesicles (SUVs), or large unilamellar vesicles (LUVs), withSUVs being preferred. The various liposome-nucleic acid complexes areprepared using methods well known in the art. See, e.g., Straubinger etal., Methods of Immunology (1983), 101:512-527, which is hereinincorporated by reference. For example, MLVs containing nucleic acid canbe prepared by depositing a thin film of phospholipid on the walls of aglass tube and subsequently hydrating with a solution of the material tobe encapsulated. SUVs are prepared by extended sonication of MLVs toproduce a homogeneous population of unilamellar liposomes. The materialto be entrapped is added to a suspension of preformed MLVs and thensonicated. When using liposomes containing cationic lipids, the driedlipid film is resuspended in an appropriate solution such as sterilewater or an isotonic buffer solution such as 10 mM Tris/NaCl, sonicated,and then the preformed liposomes are mixed directly with the DNA. Theliposome and DNA form a very stable complex due to binding of thepositively charged liposomes to the cationic DNA. SUVs find use withsmall nucleic acid fragments. LUVs are prepared by a number of methods,well known in the art. Commonly used methods include Ca²⁺-EDTA chelation(Papahadjopoulos et al., Biochim. Biophys. Acta (1975) 394:483; Wilsonet al., Cell 17:77 (1979)); ether injection (Deamer, D. and Bangham, A.,Biochim. Biophys. Acta 443:629 (1976); Ostro et al., Biochem. Biophys.Res. Commun. 76:836 (1977); Fraley et al., Proc. Natl. Acad. Sci. USA76:3348 (1979)); detergent dialysis (Enoch, H. and Strittmatter, P.,Proc. Natl. Acad. Sci. USA 76:145 (1979)); and reverse-phase evaporation(REV) (Fraley et al., J. Biol. Chem. 255:10431 (1980); Szoka, F. andPapahadjopoulos, D., Proc. Natl. Acad. Sci. USA 75:145 (1978);Schaefer-Ridder et al., Science 215:166 (1982)), which are hereinincorporated by reference.

Generally, the ratio of DNA to liposomes will be from about 10:1 toabout 1:10. Preferably, the ration will be from about 5:1 to about 1:5.More preferably, the ration will be about 3:1 to about 1:3. Still morepreferably, the ratio will be about 1:1. U.S. Pat. No. 5,676,954 (whichis herein incorporated by reference) reports on the injection of geneticmaterial, complexed with cationic liposomes carriers, into mice. U.S.Pat. Nos. 4,897,355, 4,946,787, 5,049,386, 5,459,127, 5,589,466,5,693,622, 5,580,859, 5,703,055, and international publication no. WO94/9469 (which are herein incorporated by reference) provide cationiclipids for use in transfecting DNA into cells and mammals. U.S. Pat.Nos. 5,589,466, 5,693,622, 5,580,859, 5,703,055, and internationalpublication no. WO 94/9469 provide methods for delivering DNA-cationiclipid complexes to mammals.

In certain embodiments, cells are engineered, ex vivo or in vivo, usinga retroviral particle containing RNA which comprises a sequence encodingan albumin fusion protein of the present invention. Retroviruses fromwhich the retroviral plasmid vectors may be derived include, but are notlimited to, Moloney Murine Leukemia Virus, spleen necrosis virus, Roussarcoma Virus, Harvey Sarcoma Virus, avian leukosis virus, gibbon apeleukemia virus, human immunodeficiency virus, Myeloproliferative SarcomaVirus, and mammary tumor virus.

The retroviral plasmid vector is employed to transduce packaging celllines to form producer cell lines. Examples of packaging cells which maybe transfected include, but are not limited to, the PE501, PA317, R-2,R-AM, PA12, T19-14X, VT-19-17-H2, RCRE, RCRIP, GP+E-86, GP+envAm12, andDAN cell lines as described in Miller, Human Gene Therapy 1:5-14 (1990),which is incorporated herein by reference in its entirety. The vectormay transduce the packaging cells through any means known in the art.Such means include, but are not limited to, electroporation, the use ofliposomes, and CaPO₄ precipitation. In one alternative, the retroviralplasmid vector may be encapsulated into a liposome, or coupled to alipid, and then administered to a host.

The producer cell line generates infectious retroviral vector particleswhich include polynucleotide encoding an albumin fusion protein of thepresent invention. Such retroviral vector particles then may beemployed, to transduce eukaryotic cells, either in vitro or in vivo. Thetransduced eukaryotic cells will express a fusion protein of the presentinvention.

In certain other embodiments, cells are engineered, ex vivo or in vivo,with polynucleotide contained in an adenovirus vector. Adenovirus can bemanipulated such that it encodes and expresses fusion protein of thepresent invention, and at the same time is inactivated in terms of itsability to replicate in a normal lytic viral life cycle. Adenovirusexpression is achieved without integration of the viral DNA into thehost cell chromosome, thereby alleviating concerns about insertionalmutagenesis. Furthermore, adenoviruses have been used as live entericvaccines for many years with an excellent safety profile (Schwartz etal. Am. Rev. Respir. Dis. 109:233-238 (1974)). Finally, adenovirusmediated gene transfer has been demonstrated in a number of instancesincluding transfer of alpha-1-antitrypsin and CFTR to the lungs ofcotton rats (Rosenfeld, M. A. et al. (1991) Science 252:431-434;Rosenfeld et al., (1992) Cell 68:143-155). Furthermore, extensivestudies to attempt to establish adenovirus as a causative agent in humancancer were uniformly negative (Green, M. et al. (1979) Proc. Natl.Acad. Sci. USA 76:6606).

Suitable adenoviral vectors useful in the present invention aredescribed, for example, in Kozarsky and Wilson, Curr. Opin. Genet.Devel. 3:499-503 (1993); Rosenfeld et al., Cell 68:143-155 (1992);Engelhardt et al., Human Genet. Ther. 4:759-769 (1993); Yang et al.,Nature Genet. 7:362-369 (1994); Wilson et al., Nature 365:691-692(1993); and U.S. Pat. No. 5,652,224, which are herein incorporated byreference. For example, the adenovirus vector Ad2 is useful and can begrown in human 293 cells. These cells contain the E1 region ofadenovirus and constitutively express E1a and E1b, which complement thedefective adenoviruses by providing the products of the genes deletedfrom the vector. In addition to Ad2, other varieties of adenovirus(e.g., Ad3, Ad5, and Ad7) are also useful in the present invention.

Preferably, the adenoviruses used in the present invention arereplication deficient. Replication deficient adenoviruses require theaid of a helper virus and/or packaging cell line to form infectiousparticles. The resulting virus is capable of infecting cells and canexpress a polynucleotide of interest which is operably linked to apromoter, but cannot replicate in most cells. Replication deficientadenoviruses may be deleted in one or more of all or a portion of thefollowing genes: E1a, E1b, E3, E4, E2a, or L1 through L5.

In certain other embodiments, the cells are engineered, ex vivo or invivo, using an adeno-associated virus (AAV). AAVs are naturallyoccurring defective viruses that require helper viruses to produceinfectious particles (Muzyczka, N., Curr. Topics in Microbiol. Immunol.158:97 (1992)). It is also one of the few viruses that may integrate itsDNA into non-dividing cells. Vectors containing as little as 300 basepairs of AAV can be packaged and can integrate, but space for exogenousDNA is limited to about 4.5 kb. Methods for producing and using suchAAVs are known in the art. See, for example, U.S. Pat. Nos. 5,139,941,5,173,414, 5,354,678, 5,436,146, 5,474,935, 5,478,745, and 5,589,377.

For example, an appropriate AAV vector for use in the present inventionwill include all the sequences necessary for DNA replication,encapsidation, and host-cell integration. The polynucleotide constructis inserted into the AAV vector using standard cloning methods, such asthose found in Sambrook et al., Molecular Cloning: A Laboratory Manual,Cold Spring Harbor Press (1989). The recombinant AAV vector is thentransfected into packaging cells which are infected with a helper virus,using any standard technique, including lipofection, electroporation,calcium phosphate precipitation, etc. Appropriate helper viruses includeadenoviruses, cytomegaloviruses, vaccinia viruses, or herpes viruses.Once the packaging cells are transfected and infected, they will produceinfectious AAV viral particles which contain the polynucleotideconstruct. These viral particles are then used to transduce eukaryoticcells, either ex vivo or in vivo. The transduced cells will contain thepolynucleotide construct integrated into its genome, and will express afusion protein of the invention.

Another method of gene therapy involves operably associatingheterologous control regions and endogenous polynucleotide sequences(e.g. encoding a polypeptide of the present invention) via homologousrecombination (see, e.g., U.S. Pat. No. 5,641,670, issued Jun. 24, 1997;International Publication No. WO 96/29411, published Sep. 26, 1996;International Publication No. WO 94/12650, published Aug. 4, 1994;Koller et al., Proc. Natl. Acad. Sci. USA 86:8932-8935 (1989); andZijlstra et al., Nature 342:435-438 (1989), which are hereinincorporated by reference. This method involves the activation of a genewhich is present in the target cells, but which is not normallyexpressed in the cells, or is expressed at a lower level than desired.

Polynucleotide constructs are made, using standard techniques known inthe art, which contain the promoter with targeting sequences flankingthe promoter. Suitable promoters are described herein. The targetingsequence is sufficiently complementary to an endogenous sequence topermit homologous recombination of the promoter-targeting sequence withthe endogenous sequence. The targeting sequence will be sufficientlynear the 5′ end of the desired endogenous polynucleotide sequence so thepromoter will be operably linked to the endogenous sequence uponhomologous recombination.

The promoter and the targeting sequences can be amplified using PCR.Preferably, the amplified promoter contains distinct restriction enzymesites on the 5′ and 3′ ends. Preferably, the 3′ end of the firsttargeting sequence contains the same restriction enzyme site as the 5′end of the amplified promoter and the 5′ end of the second targetingsequence contains the same restriction site as the 3′ end of theamplified promoter. The amplified promoter and targeting sequences aredigested and ligated together.

The promoter-targeting sequence construct is delivered to the cells,either as naked polynucleotide, or in conjunction withtransfection-facilitating agents, such as liposomes, viral sequences,viral particles, whole viruses, lipofection, precipitating agents, etc.,described in more detail above. The P promoter-targeting sequence can bedelivered by any method, included direct needle injection, intravenousinjection, topical administration, catheter infusion, particleaccelerators, etc. The methods are described in more detail below.

The promoter-targeting sequence construct is taken up by cells.Homologous recombination between the construct and the endogenoussequence takes place, such that an endogenous sequence is placed underthe control of the promoter. The promoter then drives the expression ofthe endogenous sequence.

The polynucleotide encoding an albumin fusion protein of the presentinvention may contain a secretory signal sequence that facilitatessecretion of the protein. Typically, the signal sequence is positionedin the coding region of the polynucleotide to be expressed towards or atthe 5′ end of the coding region. The signal sequence may be homologousor heterologous to the polynucleotide of interest and may be homologousor heterologous to the cells to be transfected. Additionally, the signalsequence may be chemically synthesized using methods known in the art.

Any mode of administration of any of the above-described polynucleotidesconstructs can be used so long as the mode results in the expression ofone or more molecules in an amount sufficient to provide a therapeuticeffect. This includes direct needle injection, systemic injection,catheter infusion, biolistic injectors, particle accelerators (i.e.,“gene guns”), gelfoam sponge depots, other commercially available depotmaterials, osmotic pumps (e.g., Alza minipumps), oral or suppositorialsolid (tablet or pill) pharmaceutical formulations, and decanting ortopical applications during surgery. For example, direct injection ofnaked calcium phosphate-precipitated plasmid into rat liver and ratspleen or a protein-coated plasmid into the portal vein has resulted ingene expression of the foreign gene in the rat livers (Kaneda et al.,Science 243:375 (1989)).

A preferred method of local administration is by direct injection.Preferably, an albumin fusion protein of the present invention complexedwith a delivery vehicle is administered by direct injection into orlocally within the area of arteries. Administration of a compositionlocally within the area of arteries refers to injecting the compositioncentimeters and preferably, millimeters within arteries.

Another method of local administration is to contact a polynucleotideconstruct of the present invention in or around a surgical wound. Forexample, a patient can undergo surgery and the polynucleotide constructcan be coated on the surface of tissue inside the wound or the constructcan be injected into areas of tissue inside the wound.

Therapeutic compositions useful in systemic administration, includefusion proteins of the present invention complexed to a targeteddelivery vehicle of the present invention. Suitable delivery vehiclesfor use with systemic administration comprise liposomes comprisingligands for targeting the vehicle to a particular site. In specificembodiments, suitable delivery vehicles for use with systemicadministration comprise liposomes comprising albumin fusion proteins ofthe invention for targeting the vehicle to a particular site.

Preferred methods of systemic administration, include intravenousinjection, aerosol, oral and percutaneous (topical) delivery.Intravenous injections can be performed using methods standard in theart. Aerosol delivery can also be performed using methods standard inthe art (see, for example, Stribling et al., Proc. Natl. Acad. Sci. USA189:11277-11281, 1992, which is incorporated herein by reference). Oraldelivery can be performed by complexing a polynucleotide construct ofthe present invention to a carrier capable of withstanding degradationby digestive enzymes in the gut of an animal. Examples of such carriers,include plastic capsules or tablets, such as those known in the art.Topical delivery can be performed by mixing a polynucleotide constructof the present invention with a lipophilic reagent (e.g., DMSO) that iscapable of passing into the skin.

Determining an effective amount of substance to be delivered can dependupon a number of factors including, for example, the chemical structureand biological activity of the substance, the age and weight of theanimal, the precise condition requiring treatment and its severity, andthe route of administration. The frequency of treatments depends upon anumber of factors, such as the amount of polynucleotide constructsadministered per dose, as well as the health and history of the subject.The precise amount, number of doses, and timing of doses will bedetermined by the attending physician or veterinarian.

Albumin fusion proteins of the present invention can be administered toany animal, preferably to mammals and birds. Preferred mammals includehumans, dogs, cats, mice, rats, rabbits sheep, cattle, horses and pigs,with humans being particularly preferred.

Biological Activities

Albumin fusion proteins and/or polynucleotides encoding albumin fusionproteins of the present invention, can be used in assays to test for oneor more biological activities. If an albumin fusion protein and/orpolynucleotide exhibits an activity in a particular assay, it is likelythat the Therapeutic protein corresponding to the fusion protein may beinvolved in the diseases associated with the biological activity. Thus,the fusion protein could be used to treat the associated disease.

In preferred embodiments, the present invention encompasses a method oftreating a disease or disorder listed in the “Preferred Indication Y”column of Table 1 comprising administering to a patient in which suchtreatment, prevention or amelioration is desired an albumin fusionprotein of the invention that comprises a Therapeutic protein portioncorresponding to a Therapeutic protein disclosed in the “TherapeuticProtein X” column of Table 1 (in the same row as the disease or disorderto be treated is listed in the “Preferred Indication Y” column ofTable 1) in an amount effective to treat, prevent or ameliorate thedisease or disorder.

In a further preferred embodiment, the present invention encompasses amethod of treating a disease or disorder listed for a particularTherapeutic protein in the “Preferred Indication:Y” column of Table 1comprising administering to a patient in which such treatment,prevention or amelioration is desired an albumin fusion protein of theinvention that comprises a Therapeutic protein portion corresponding tothe Therapeutic protein for which the indications in the Examples arerelated in an amount effective to treat, prevent or ameliorate thedisease or disorder.

Specifically contemplated by the present invention are albumin fusionproteins produced by a cell when encoded by the polynucleotides thatencode SEQ ID NO:Y. When these polynucleotides are used to express theencoded protein from a cell, the cell's natural secretion and processingsteps produces a protein that lacks the signal sequence explicitlylisted in columns 4 and/or 11 of Table 2. The specific amino acidsequence of the listed signal sequence is shown in the specification oris well known in the art. Thus, most preferred embodiments of thepresent invention include the albumin fusion protein produced by a cell(which would lack the leader sequence shown in columns 4 and/or 11 ofTable 2). Also most preferred are polypeptides comprising SEQ ID NO:Ywithout the specific leader sequence listed in columns 4 and/or 11 ofTable 2. Compositions comprising these two preferred embodiments,including pharmaceutical compositions, are also preferred. These albuminfusion proteins are specifically contemplated to treat, prevent, orameliorate a disease or disorder listed for a particular Therapeuticprotein in the “Preferred Indication:Y” column of Table 1.

In preferred embodiments, fusion proteins of the present invention maybe used in the diagnosis, prognosis, prevention and/or treatment ofdiseases and/or disorders relating to diseases and disorders of theendocrine system (see, for example, “Endocrine Disorders” sectionbelow), the nervous system (see, for example, “Neurological Disorders”section below), the immune system (see, for example, “Immune Activity”section below), respiratory system (see, for example, “RespiratoryDisorders” section below), cardiovascular system (see, for example,“Cardiovascular Disorders” section below), reproductive system (see, forexample, “Reproductive System Disorders” section below) digestive system(see, for example, “Gastrointestinal Disorders” section below), diseasesand/or disorders relating to cell proliferation (see, for example,“Hyperproliferative Disorders” section below), and/or diseases ordisorders relating to the blood (see, for example, “Blood-RelatedDisorders” section below).

In certain embodiments, an albumin fusion protein of the presentinvention may be used to diagnose and/or prognose diseases and/ordisorders associated with the tissue(s) in which the gene correspondingto the Therapeutic protein portion of the fusion protein of theinvention is expressed.

Thus, fusion proteins of the invention and polynucleotides encodingalbumin fusion proteins of the invention are useful in the diagnosis,detection and/or treatment of diseases and/or disorders associated withactivities that include, but are not limited to, prohormone activation,neurotransmitter activity, cellular signaling, cellular proliferation,cellular differentiation, and cell migration.

More generally, fusion proteins of the invention and polynucleotidesencoding albumin fusion proteins of the invention may be useful for thediagnosis, prognosis, prevention and/or treatment of diseases and/ordisorders associated with the following systems.

Immune Activity

Albumin fusion proteins of the invention and polynucleotides encodingalbumin fusion proteins of the invention may be useful in treating,preventing, diagnosing and/or prognosing diseases, disorders, and/orconditions of the immune system, by, for example, activating orinhibiting the proliferation, differentiation, or mobilization(chemotaxis) of immune cells. Immune cells develop through a processcalled hematopoiesis, producing myeloid (platelets, red blood cells,neutrophils, and macrophages) and lymphoid (B and T lymphocytes) cellsfrom pluripotent stem cells. The etiology of these immune diseases,disorders, and/or conditions may be genetic, somatic, such as cancer andsome autoimmune diseases, acquired (e.g., by chemotherapy or toxins), orinfectious. Moreover, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention can beused as a marker or detector of a particular immune system disease ordisorder.

In another embodiment, a fusion protein of the invention and/orpolynucleotide encoding an albumin fusion protein of the invention, maybe used to treat diseases and disorders of the immune system and/or toinhibit or enhance an immune response generated by cells associated withthe tissue(s) in which the polypeptide of the invention is expressed.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in treating,preventing, diagnosing, and/or prognosing immunodeficiencies, includingboth congenital and acquired immunodeficiencies. Examples of B cellimmunodeficiencies in which immunoglobulin levels B cell function and/orB cell numbers are decreased include: X-linked agammaglobulinemia(Bruton's disease), X-linked infantile agammaglobulinemia, X-linkedimmunodeficiency with hyper IgM, non X-linked immunodeficiency withhyper IgM, X-linked lymphoproliferative syndrome (XLP),agammaglobulinemia including congenital and acquired agammaglobulinemia,adult onset agammaglobulinemia, late-onset agammaglobulinemia,dysgammaglobulinemia, hypogammaglobulinemia, unspecifiedhypogammaglobulinemia, recessive agammaglobulinemia (Swiss type),Selective IgM deficiency, selective IgA deficiency, selective IgGsubclass deficiencies, IgG subclass deficiency (with or without IgAdeficiency), Ig deficiency with increased IgM, IgG and IgA deficiencywith increased IgM, antibody deficiency with normal or elevated Igs, Igheavy chain deletions, kappa chain deficiency, B celllymphoproliferative disorder (BLPD), common variable immunodeficiency(CVID), common variable immunodeficiency (CVI) (acquired), and transienthypogammaglobulinemia of infancy.

In specific embodiments, ataxia-telangiectasia or conditions associatedwith ataxia-telangiectasia are treated, prevented, diagnosed, and/orprognosing using the, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention.

Examples of congenital immunodeficiencies in which T cell and/or B cellfunction and/or number is decreased include, but are not limited to:DiGeorge anomaly, severe combined immunodeficiencies (SCID) (including,but not limited to, X-linked SCID, autosomal recessive SCID, adenosinedeaminase deficiency, purine nucleoside phosphorylase (PNP) deficiency,Class II MHC deficiency (Bare lymphocyte syndrome), Wiskott-Aldrichsyndrome, and ataxia telangiectasia), thymic hypoplasia, third andfourth pharyngeal pouch syndrome, 22q11.2 deletion, chronicmucocutaneous candidiasis, natural killer cell deficiency (NK),idiopathic CD4+ T-lymphocytopenia, immunodeficiency with predominant Tcell defect (unspecified), and unspecified immunodeficiency of cellmediated immunity.

In specific embodiments, DiGeorge anomaly or conditions associated withDiGeorge anomaly are treated, prevented, diagnosed, and/or prognosedusing fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention.

Other immunodeficiencies that may be treated, prevented, diagnosed,and/or prognosed using fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention,include, but are not limited to, chronic granulomatous disease,Chédiak-Higashi syndrome, myeloperoxidase deficiency, leukocyteglucose-6-phosphate dehydrogenase deficiency, X-linkedlymphoproliferative syndrome (XLP), leukocyte adhesion deficiency,complement component deficiencies (including C1, C2, C3, C4, C5, C6, C7,C8 and/or C9 deficiencies), reticular dysgenesis, thymicalymphoplasia-aplasia, immunodeficiency with thymoma, severe congenitalleukopenia, dysplasia with immunodeficiency, neonatal neutropenia, shortlimbed dwarfism, and Nezelof syndrome-combined immunodeficiency withIgs.

In a preferred embodiment, the immunodeficiencies and/or conditionsassociated with the immunodeficiencies recited above are treated,prevented, diagnosed and/or prognosed using fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention.

In a preferred embodiment fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention couldbe used as an agent to boost immunoresponsiveness among immunodeficientindividuals. In specific embodiments, fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventioncould be used as an agent to boost immunoresponsiveness among B celland/or T cell immunodeficient individuals.

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be useful intreating, preventing, diagnosing and/or prognosing autoimmune disorders.Many autoimmune disorders result from inappropriate recognition of selfas foreign material by immune cells. This inappropriate recognitionresults in an immune response leading to the destruction of the hosttissue. Therefore, the administration of fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention that can inhibit an immune response, particularly theproliferation, differentiation, or chemotaxis of T-cells, may be aneffective therapy in preventing autoimmune disorders.

Autoimmune diseases or disorders that may be treated, prevented,diagnosed and/or prognosed by fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventioninclude, but are not limited to, one or more of the following: systemiclupus erythematosus, rheumatoid arthritis, ankylosing spondylitis,multiple sclerosis, autoimmune thyroiditis, Hashimoto's thyroiditis,autoimmune hemolytic anemia, hemolytic anemia, thrombocytopenia,autoimmune thrombocytopenia purpura, autoimmune neonatalthrombocytopenia, idiopathic thrombocytopenia purpura, purpura (e.g.,Henloch-Scoenlein purpura), autoimmunocytopenia, Goodpasture's syndrome,Pemphigus vulgaris, myasthenia gravis, Grave's disease(hyperthyroidism), and insulin-resistant diabetes mellitus.

Additional disorders that are likely to have an autoimmune componentthat may be treated, prevented, and/or diagnosed with the albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention include, but are not limited to, type IIcollagen-induced arthritis, antiphospholipid syndrome, dermatitis,allergic encephalomyelitis, myocarditis, relapsing polychondritis,rheumatic heart disease, neuritis, uveitis ophthalmia,polyendocrinopathies, Reiter's Disease, Stiff-Man Syndrome, autoimmunepulmonary inflammation, autism, Guillain-Barre Syndrome, insulindependent diabetes mellitus, and autoimmune inflammatory eye disorders.

Additional disorders that are likely to have an autoimmune componentthat may be treated, prevented, diagnosed and/or prognosed with thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention include, but are not limitedto, scleroderma with anti-collagen antibodies (often characterized,e.g., by nucleolar and other nuclear antibodies), mixed connectivetissue disease (often characterized, e.g., by antibodies to extractablenuclear antigens (e.g., ribonucleoprotein)), polymyositis (oftencharacterized, e.g., by nonhistone ANA), pernicious anemia (oftencharacterized, e.g., by antiparietal cell, microsomes, and intrinsicfactor antibodies), idiopathic Addison's disease (often characterized,e.g., by humoral and cell-mediated adrenal cytotoxicity, infertility(often characterized, e.g., by antispermatozoal antibodies),glomerulonephritis (often characterized, e.g., by glomerular basementmembrane antibodies or immune complexes), bullous pemphigoid (oftencharacterized, e.g., by IgG and complement in basement membrane),Sjogren's syndrome (often characterized, e.g., by multiple tissueantibodies, and/or a specific nonhistone ANA (SS-B)), diabetes mellitus(often characterized, e.g., by cell-mediated and humoral islet cellantibodies), and adrenergic drug resistance (including adrenergic drugresistance with asthma or cystic fibrosis) (often characterized, e.g.,by beta-adrenergic receptor antibodies).

Additional disorders that may have an autoimmune component that may betreated, prevented, diagnosed and/or prognosed with the albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention include, but are not limited to, chronicactive hepatitis (often characterized, e.g., by smooth muscleantibodies), primary biliary cirrhosis (often characterized, e.g., bymitochondria antibodies), other endocrine gland failure (oftencharacterized, e.g., by specific tissue antibodies in some cases),vitiligo (often characterized, e.g., by melanocyte antibodies),vasculitis (often characterized, e.g., by Ig and complement in vesselwalls and/or low serum complement), post-MI (often characterized, e.g.,by myocardial antibodies), cardiotomy syndrome (often characterized,e.g., by myocardial antibodies), urticaria (often characterized, e.g.,by IgG and IgM antibodies to IgE), atopic dermatitis (oftencharacterized, e.g., by IgG and IgM antibodies to IgE), asthma (oftencharacterized, e.g., by IgG and IgM antibodies to IgE), and many otherinflammatory, granulomatous, degenerative, and atrophic disorders.

In a preferred embodiment, the autoimmune diseases and disorders and/orconditions associated with the diseases and disorders recited above aretreated, prevented, diagnosed and/or prognosed using for example, fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention. In a specific preferred embodiment,rheumatoid arthritis is treated, prevented, and/or diagnosed usingfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention.

In another specific preferred embodiment, systemic lupus erythematosusis treated, prevented, and/or diagnosed using fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention. In another specific preferred embodiment, idiopathicthrombocytopenia purpura is treated, prevented, and/or diagnosed usingfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention.

In another specific preferred embodiment IgA nephropathy is treated,prevented, and/or diagnosed using fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention.

In a preferred embodiment, the autoimmune diseases and disorders and/orconditions associated with the diseases and disorders recited above aretreated, prevented, diagnosed and/or prognosed using fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention.

In preferred embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused as a immunosuppressive agent(s).

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in treating,preventing, prognosing, and/or diagnosing diseases, disorders, and/orconditions of hematopoietic cells. Albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention could be used to increase differentiation and proliferation ofhematopoietic cells, including the pluripotent stem cells, in an effortto treat or prevent those diseases, disorders, and/or conditionsassociated with a decrease in certain (or many) types hematopoieticcells, including but not limited to, leukopenia, neutropenia, anemia,and thrombocytopenia. Alternatively, fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventioncould be used to increase differentiation and proliferation ofhematopoietic cells, including the pluripotent stem cells, in an effortto treat or prevent those diseases, disorders, and/or conditionsassociated with an increase in certain (or many) types of hematopoieticcells, including but not limited to, histiocytosis.

Allergic reactions and conditions, such as asthma (particularly allergicasthma) or other respiratory problems, may also be treated, prevented,diagnosed and/or prognosed using fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention.Moreover, these molecules can be used to treat, prevent, prognose,and/or diagnose anaphylaxis, hypersensitivity to an antigenic molecule,or blood group incompatibility.

Additionally, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, may be used to treat,prevent, diagnose and/or prognose IgE-mediated allergic reactions. Suchallergic reactions include, but are not limited to, asthma, rhinitis,and eczema. In specific embodiments, fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be used to modulate IgE concentrations in vitro or in vivo.

Moreover, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention have uses in thediagnosis, prognosis, prevention, and/or treatment of inflammatoryconditions. For example, since fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention mayinhibit the activation, proliferation and/or differentiation of cellsinvolved in an inflammatory response, these molecules can be used toprevent and/or treat chronic and acute inflammatory conditions. Suchinflammatory conditions include, but are not limited to, for example,inflammation associated with infection (e.g., septic shock, sepsis, orsystemic inflammatory response syndrome), ischemia-reperfusion injury,endotoxin lethality, complement-mediated hyperacute rejection,nephritis, cytokine or chemokine induced lung injury, inflammatory boweldisease, Crohn's disease, over production of cytokines (e.g., TNF orIL-1.), respiratory disorders (e.g., asthma and allergy);gastrointestinal disorders (e.g., inflammatory bowel disease); cancers(e.g., gastric, ovarian, lung, bladder, liver, and breast); CNSdisorders (e.g., multiple sclerosis; ischemic brain injury and/orstroke, traumatic brain injury, neurodegenerative disorders (e.g.,Parkinson's disease and Alzheimer's disease); AIDS-related dementia; andprion disease); cardiovascular disorders (e.g., atherosclerosis,myocarditis, cardiovascular disease, and cardiopulmonary bypasscomplications); as well as many additional diseases, conditions, anddisorders that are characterized by inflammation (e.g., hepatitis,rheumatoid arthritis, gout, trauma, pancreatitis, sarcoidosis,dermatitis, renal ischemia-reperfusion injury, Grave's disease, systemiclupus erythematosus, diabetes mellitus, and allogenic transplantrejection).

Because inflammation is a fundamental defense mechanism, inflammatorydisorders can effect virtually any tissue of the body. Accordingly,fusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention, have uses in the treatment oftissue-specific inflammatory disorders, including, but not limited to,adrenalitis, alveolitis, angiocholecystitis, appendicitis, balanitis,blepharitis, bronchitis, bursitis, carditis, cellulitis, cervicitis,cholecystitis, chorditis, cochlitis, colitis, conjunctivitis, cystitis,dermatitis, diverticulitis, encephalitis, endocarditis, esophagitis,eustachitis, fibrositis, folliculitis, gastritis, gastroenteritis,gingivitis, glossitis, hepatosplenitis, keratitis, labyrinthitis,laryngitis, lymphangitis, mastitis, media otitis, meningitis, metritis,mucitis, myocarditis, myosititis, myringitis, nephritis, neuritis,orchitis, osteochondritis, otitis, pericarditis, peritendonitis,peritonitis, pharyngitis, phlebitis, poliomyelitis, prostatitis,pulpitis, retinitis, rhinitis, salpingitis, scleritis,sclerochoroiditis, scrotitis, sinusitis, spondylitis, steatitis,stomatitis, synovitis, syringitis, tendonitis, tonsillitis, urethritis,and vaginitis.

In specific embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, areuseful to diagnose, prognose, prevent, and/or treat organ transplantrejections and graft-versus-host disease. Organ rejection occurs by hostimmune cell destruction of the transplanted tissue through an immuneresponse. Similarly, an immune response is also involved in GVHD, but,in this case, the foreign transplanted immune cells destroy the hosttissues. Polypeptides, antibodies, or polynucleotides of the invention,and/or agonists or antagonists thereof, that inhibit an immune response,particularly the activation, proliferation, differentiation, orchemotaxis of T-cells, may be an effective therapy in preventing organrejection or GVHD. In specific embodiments, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention, that inhibit an immune response, particularly the activation,proliferation, differentiation, or chemotaxis of T-cells, may be aneffective therapy in preventing experimental allergic and hyperacutexenograft rejection.

In other embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, areuseful to diagnose, prognose, prevent, and/or treat immune complexdiseases, including, but not limited to, serum sickness, poststreptococcal glomerulonephritis, polyarteritis nodosa, and immunecomplex-induced vasculitis.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention can be used to treat, detect,and/or prevent infectious agents. For example, by increasing the immuneresponse, particularly increasing the proliferation activation and/ordifferentiation of B and/or T cells, infectious diseases may be treated,detected, and/or prevented. The immune response may be increased byeither enhancing an existing immune response, or by initiating a newimmune response. Alternatively, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention mayalso directly inhibit the infectious agent (refer to section ofapplication listing infectious agents, etc), without necessarilyeliciting an immune response.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused as a vaccine adjuvant that enhances immune responsiveness to anantigen. In a specific embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used as an adjuvant to enhance tumor-specific immuneresponses.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an adjuvant to enhance anti-viral immune responses.Anti-viral immune responses that may be enhanced using the compositionsof the invention as an adjuvant, include virus and virus associateddiseases or symptoms described herein or otherwise known in the art. Inspecific embodiments, the compositions of the invention are used as anadjuvant to enhance an immune response to a virus, disease, or symptomselected from the group consisting of: AIDS, meningitis, Dengue, EBV,and hepatitis (e.g., hepatitis B). In another specific embodiment, thecompositions of the invention are used as an adjuvant to enhance animmune response to a virus, disease, or symptom selected from the groupconsisting of: HIV/AIDS, respiratory syncytial virus, Dengue, rotavirus,Japanese B encephalitis, influenza A and B, parainfluenza, measles,cytomegalovirus, rabies, Junin, Chikungunya, Rift Valley Fever, herpessimplex, and yellow fever.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an adjuvant to enhance anti-bacterial or anti-fungal immuneresponses. Anti-bacterial or anti-fungal immune responses that may beenhanced using the compositions of the invention as an adjuvant, includebacteria or fungus and bacteria or fungus associated diseases orsymptoms described herein or otherwise known in the art. In specificembodiments, the compositions of the invention are used as an adjuvantto enhance an immune response to a bacteria or fungus, disease, orsymptom selected from the group consisting of: tetanus, Diphtheria,botulism, and meningitis type B.

In another specific embodiment, the compositions of the invention areused as an adjuvant to enhance an immune response to a bacteria orfungus, disease, or symptom selected from the group consisting of:Vibrio cholerae, Mycobacterium leprae, Salmonella typhi, Salmonellaparatyphi, Meisseria meningitidis, Streptococcus pneumoniae, Group Bstreptococcus, Shigella spp., Enterotoxigenic Escherichia coli,Enterohemorrhagic E. coli, and Borrelia burgdorferi.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an adjuvant to enhance anti-parasitic immune responses.Anti-parasitic immune responses that may be enhanced using thecompositions of the invention as an adjuvant, include parasite andparasite associated diseases or symptoms described herein or otherwiseknown in the art. In specific embodiments, the compositions of theinvention are used as an adjuvant to enhance an immune response to aparasite. In another specific embodiment, the compositions of theinvention are used as an adjuvant to enhance an immune response toPlasmodium (malaria) or Leishmania.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay also be employed to treat infectious diseases including silicosis,sarcoidosis, and idiopathic pulmonary fibrosis; for example, bypreventing the recruitment and activation of mononuclear phagocytes.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an antigen for the generation of antibodies to inhibit orenhance immune mediated responses against polypeptides of the invention.

In one embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areadministered to an animal (e.g., mouse, rat, rabbit, hamster, guineapig, pigs, micro-pig, chicken, camel, goat, horse, cow, sheep, dog, cat,non-human primate, and human, most preferably human) to boost the immunesystem to produce increased quantities of one or more antibodies (e.g.,IgG, IgA, IgM, and IgE), to induce higher affinity antibody productionand immunoglobulin class switching (e.g., IgG, IgA, IgM, and IgE),and/or to increase an immune response.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a stimulator of B cell responsiveness to pathogens.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an activator of T cells.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent that elevates the immune status of an individualprior to their receipt of immunosuppressive therapies.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to induce higher affinity antibodies.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to increase serum immunoglobulin concentrations.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to accelerate recovery of immunocompromisedindividuals.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to boost immunoresponsiveness among agedpopulations and/or neonates.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an immune system enhancer prior to, during, or after bonemarrow transplant and/or other transplants (e.g., allogeneic orxenogeneic organ transplantation). With respect to transplantation,compositions of the invention may be administered prior to, concomitantwith, and/or after transplantation. In a specific embodiment,compositions of the invention are administered after transplantation,prior to the beginning of recovery of T-cell populations. In anotherspecific embodiment, compositions of the invention are firstadministered after transplantation after the beginning of recovery of Tcell populations, but prior to full recovery of B cell populations.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to boost immunoresponsiveness among individualshaving an acquired loss of B cell function. Conditions resulting in anacquired loss of B cell function that may be ameliorated or treated byadministering the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention,include, but are not limited to, HIV Infection, AIDS, bone marrowtransplant, and B cell chronic lymphocytic leukemia (CLL).

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to boost immunoresponsiveness among individualshaving a temporary immune deficiency. Conditions resulting in atemporary immune deficiency that may be ameliorated or treated byadministering the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention,include, but are not limited to, recovery from viral infections (e.g.,influenza), conditions associated with malnutrition, recovery frominfectious mononucleosis, or conditions associated with stress, recoveryfrom measles, recovery from blood transfusion, and recovery fromsurgery.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a regulator of antigen presentation by monocytes, dendriticcells, and/or B-cells. In one embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention enhance antigen presentation or antagonize antigenpresentation in vitro or in vivo. Moreover, in related embodiments, thisenhancement or antagonism of antigen presentation may be useful as ananti-tumor treatment or to modulate the immune system.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as an agent to direct an individual's immune system towardsdevelopment of a humoral response (i.e. TH2) as opposed to a TH1cellular response.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a means to induce tumor proliferation and thus make it moresusceptible to anti-neoplastic agents. For example, multiple myeloma isa slowly dividing disease and is thus refractory to virtually allanti-neoplastic regimens. If these cells were forced to proliferate morerapidly their susceptibility profile would likely change.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a stimulator of B cell production in pathologies such asAIDS, chronic lymphocyte disorder and/or Common VariableImmunodificiency.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a therapy for generation and/or regeneration of lymphoidtissues following surgery, trauma or genetic defect. In another specificembodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused in the pretreatment of bone marrow samples prior to transplant.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a gene-based therapy for genetically inherited disordersresulting in immuno-incompetence/immunodeficiency such as observed amongSCID patients.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a means of activating monocytes/macrophages to defendagainst parasitic diseases that effect monocytes such as Leishmania.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a means of regulating secreted cytokines that are elicitedby polypeptides of the invention.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused in one or more of the applications described herein, as they mayapply to veterinary medicine.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a means of blocking various aspects of immune responses toforeign agents or self. Examples of diseases or conditions in whichblocking of certain aspects of immune responses may be desired includeautoimmune disorders such as lupus, and arthritis, as well asimmunoresponsiveness to skin allergies, inflammation, bowel disease,injury and diseases/disorders associated with pathogens.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a therapy for preventing the B cell proliferation and Igsecretion associated with autoimmune diseases such as idiopathicthrombocytopenic purpura, systemic lupus erythematosus and multiplesclerosis.

In another specific embodiment, polypeptides, antibodies,polynucleotides and/or agonists or antagonists of the present fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention are used as a inhibitor of B and/or T cellmigration in endothelial cells. This activity disrupts tissuearchitecture or cognate responses and is useful, for example indisrupting immune responses, and blocking sepsis.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a therapy for chronic hypergammaglobulinemia evident in suchdiseases as monoclonal gammopathy of undetermined significance (MGUS),Waldenstrom's disease, related idiopathic monoclonal gammopathies, andplasmacytomas.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be employed for instance to inhibit polypeptide chemotaxis andactivation of macrophages and their precursors, and of neutrophils,basophils, B lymphocytes and some T-cell subsets, e.g., activated andCD8 cytotoxic T cells and natural killer cells, in certain autoimmuneand chronic inflammatory and infective diseases. Examples of autoimmunediseases are described herein and include multiple sclerosis, andinsulin-dependent diabetes.

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may also be employedto treat idiopathic hyper-eosinophilic syndrome by, for example,preventing eosinophil production and migration.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used to enhance or inhibit complement mediated cell lysis.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used to enhance or inhibit antibody dependent cellular cytotoxicity.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay also be employed for treating atherosclerosis, for example, bypreventing monocyte infiltration in the artery wall.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be employed to treat adult respiratory distress syndrome (ARDS).

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful for stimulating wound and tissue repair, stimulatingangiogenesis, and/or stimulating the repair of vascular or lymphaticdiseases or disorders. Additionally, fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be used to stimulate the regeneration of mucosal surfaces.

In a specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used to diagnose, prognose, treat, and/or prevent a disordercharacterized by primary or acquired immunodeficiency, deficient serumimmunoglobulin production, recurrent infections, and/or immune systemdysfunction. Moreover, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beused to treat or prevent infections of the joints, bones, skin, and/orparotid glands, blood-borne infections (e.g., sepsis, meningitis, septicarthritis, and/or osteomyelitis), autoimmune diseases (e.g., thosedisclosed herein), inflammatory disorders, and malignancies, and/or anydisease or disorder or condition associated with these infections,diseases, disorders and/or malignancies) including, but not limited to,CVID, other primary immune deficiencies, HIV disease, CLL, recurrentbronchitis, sinusitis, otitis media, conjunctivitis, pneumonia,hepatitis, meningitis, herpes zoster (e.g., severe herpes zoster),and/or pneumocystis carnii. Other diseases and disorders that may beprevented, diagnosed, prognosed, and/or treated with fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention include, but are not limited to, HIV infection, HTLV-BLVinfection, lymphopenia, phagocyte bactericidal dysfunction anemia,thrombocytopenia, and hemoglobinuria.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to treat, and/or diagnose an individual having common variableimmunodeficiency disease (“CVID”; also known as “acquiredagammaglobulinemia” and “acquired hypogammaglobulinemia”) or a subset ofthis disease.

In a specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be used to diagnose, prognose, prevent, and/or treat cancers orneoplasms including immune cell or immune tissue-related cancers orneoplasms. Examples of cancers or neoplasms that may be prevented,diagnosed, or treated by fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventioninclude, but are not limited to, acute myelogenous leukemia, chronicmyelogenous leukemia, Hodgkin's disease, non-Hodgkin's lymphoma, acutelymphocytic anemia (ALL) Chronic lymphocyte leukemia, plasmacytomas,multiple myeloma, Burkitt's lymphoma, EBV-transformed diseases, and/ordiseases and disorders described in the section entitled“Hyperproliferative Disorders” elsewhere herein.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a therapy for decreasing cellular proliferation of LargeB-cell Lymphomas.

In another specific embodiment, albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used as a means of decreasing the involvement of B cells and Igassociated with Chronic Myelogenous Leukemia.

In specific embodiments, the compositions of the invention are used asan agent to boost immunoresponsiveness among B cell immunodeficientindividuals, such as, for example, an individual who has undergone apartial or complete splenectomy.

Blood-Related Disorders

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be used tomodulate hemostatic (the stopping of bleeding) or thrombolytic (clotdissolving) activity. For example, by increasing hemostatic orthrombolytic activity, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention couldbe used to treat or prevent blood coagulation diseases, disorders,and/or conditions (e.g., afibrinogenemia, factor deficiencies,hemophilia), blood platelet diseases, disorders, and/or conditions(e.g., thrombocytopenia), or wounds resulting from trauma, surgery, orother causes. Alternatively, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention thatcan decrease hemostatic or thrombolytic activity could be used toinhibit or dissolve clotting. These molecules could be important in thetreatment or prevention of heart attacks (infarction), strokes, orscarring.

In specific embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be used to prevent, diagnose, prognose, and/or treat thrombosis,arterial thrombosis, venous thrombosis, thromboembolism, pulmonaryembolism, atherosclerosis, myocardial infarction, transient ischemicattack, unstable angina. In specific embodiments, the albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention may be used for the prevention of occlusion ofsaphenous grafts, for reducing the risk of periprocedural thrombosis asmight accompany angioplasty procedures, for reducing the risk of strokein patients with atrial fibrillation including nonrheumatic atrialfibrillation, for reducing the risk of embolism associated withmechanical heart valves and or mitral valves disease. Other uses for thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, include, but are not limitedto, the prevention of occlusions in extracorporeal devices (e.g.,intravascular cannulas, vascular access shunts in hemodialysis patients,hemodialysis machines, and cardiopulmonary bypass machines).

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, maybe used to prevent, diagnose, prognose, and/or treat diseases anddisorders of the blood and/or blood forming organs associated with thetissue(s) in which the polypeptide of the invention is expressed.

The fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be used to modulatehematopoietic activity (the formation of blood cells). For example, thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be used to increase thequantity of all or subsets of blood cells, such as, for example,erythrocytes, lymphocytes (B or T cells), myeloid cells (e.g.,basophils, eosinophils, neutrophils, mast cells, macrophages) andplatelets. The ability to decrease the quantity of blood cells orsubsets of blood cells may be useful in the prevention, detection,diagnosis and/or treatment of anemias and leukopenias described below.Alternatively, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beused to decrease the quantity of all or subsets of blood cells, such as,for example, erythrocytes, lymphocytes (B or T cells), myeloid cells(e.g., basophils, eosinophils, neutrophils, mast cells, macrophages) andplatelets. The ability to decrease the quantity of blood cells orsubsets of blood cells may be useful in the prevention, detection,diagnosis and/or treatment of leukocytoses, such as, for exampleeosinophilia.

The fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be used to prevent, treat,or diagnose blood dyscrasia.

Anemias are conditions in which the number of red blood cells or amountof hemoglobin (the protein that carries oxygen) in them is below normal.Anemia may be caused by excessive bleeding, decreased red blood cellproduction, or increased red blood cell destruction (hemolysis). Thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in treating,preventing, and/or diagnosing anemias. Anemias that may be treatedprevented or diagnosed by the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventioninclude iron deficiency anemia, hypochromic anemia, microcytic anemia,chlorosis, hereditary sideroblastic anemia, idiopathic acquiredsideroblastic anemia, red cell aplasia, megaloblastic anemia (e.g.,pernicious anemia, (vitamin B12 deficiency) and folic acid deficiencyanemia), aplastic anemia, hemolytic anemias (e.g., autoimmune helolyticanemia, microangiopathic hemolytic anemia, and paroxysmal nocturnalhemoglobinuria). The albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beuseful in treating, preventing, and/or diagnosing anemias associatedwith diseases including but not limited to, anemias associated withsystemic lupus erythematosus, cancers, lymphomas, chronic renal disease,and enlarged spleens. The albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in treating, preventing, and/or diagnosing anemias arisingfrom drug treatments such as anemias associated with methyldopa,dapsone, and/or sulfadrugs. Additionally, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may be useful in treating, preventing, and/or diagnosinganemias associated with abnormal red blood cell architecture includingbut not limited to, hereditary spherocytosis, hereditary elliptocytosis,glucose-6-phosphate dehydrogenase deficiency, and sickle cell anemia.

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be useful intreating, preventing, and/or diagnosing hemoglobin abnormalities, (e.g.,those associated with sickle cell anemia, hemoglobin C disease,hemoglobin S-C disease, and hemoglobin E disease). Additionally, thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in diagnosing,prognosing, preventing, and/or treating thalassemias, including, but notlimited to, major and minor forms of alpha-thalassemia andbeta-thalassemia.

In another embodiment, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in diagnosing, prognosing, preventing, and/or treatingbleeding disorders including, but not limited to, thrombocytopenia(e.g., idiopathic thrombocytopenic purpura, and thromboticthrombocytopenic purpura), Von Willebrand's disease, hereditary plateletdisorders (e.g., storage pool disease such as Chediak-Higashi andHermansky-Pudlak syndromes, thromboxane A2 dysfunction, thromboasthenia,and Bernard-Soulier syndrome), hemolytic-uremic syndrome, hemopheliassuch as hemophelia A or Factor VII deficiency and Christmas disease orFactor IX deficiency, Hereditary Hemorrhagic Telangiectsia, also knownas Rendu-Osler-Weber syndrome, allergic purpura (Henoch Schonleinpurpura) and disseminated intravascular coagulation.

The effect of the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention on theclotting time of blood may be monitored using any of the clotting testsknown in the art including, but not limited to, whole blood partialthromboplastin time (PTT), the activated partial thromboplastin time(aPTT), the activated clotting time (ACT), the recalcified activatedclotting time, or the Lee-White Clotting time.

Several diseases and a variety of drugs can cause platelet dysfunction.Thus, in a specific embodiment, the albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may be useful in diagnosing, prognosing, preventing, and/ortreating acquired platelet dysfunction such as platelet dysfunctionaccompanying kidney failure, leukemia, multiple myeloma, cirrhosis ofthe liver, and systemic lupus erythematosus as well as plateletdysfunction associated with drug treatments, including treatment withaspirin, ticlopidine, nonsteroidal anti-inflammatory drugs (used forarthritis, pain, and sprains), and penicillin in high doses.

In another embodiment, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in diagnosing, prognosing, preventing, and/or treatingdiseases and disorders characterized by or associated with increased ordecreased numbers of white blood cells. Leukopenia occurs when thenumber of white blood cells decreases below normal. Leukopenias include,but are not limited to, neutropenia and lymphocytopenia. An increase inthe number of white blood cells compared to normal is known asleukocytosis. The body generates increased numbers of white blood cellsduring infection. Thus, leukocytosis may simply be a normalphysiological parameter that reflects infection. Alternatively,leukocytosis may be an indicator of injury or other disease such ascancer. Leokocytoses, include but are not limited to, eosinophilia, andaccumulations of macrophages. In specific embodiments, the albuminfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention may be useful in diagnosing,prognosing, preventing, and/or treating leukopenia. In other specificembodiments, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beuseful in diagnosing, prognosing, preventing, and/or treatingleukocytosis.

Leukopenia may be a generalized decreased in all types of white bloodcells, or may be a specific depletion of particular types of white bloodcells. Thus, in specific embodiments, the albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may be useful in diagnosing, prognosing, preventing, and/ortreating decreases in neutrophil numbers, known as neutropenia.Neutropenias that may be diagnosed, prognosed, prevented, and/or treatedby the albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention include, but are notlimited to, infantile genetic agranulocytosis, familial neutropenia,cyclic neutropenia, neutropenias resulting from or associated withdietary deficiencies (e.g., vitamin B 12 deficiency or folic aciddeficiency), neutropenias resulting from or associated with drugtreatments (e.g., antibiotic regimens such as penicillin treatment,sulfonamide treatment, anticoagulant treatment, anticonvulsant drugs,anti-thyroid drugs, and cancer chemotherapy), and neutropenias resultingfrom increased neutrophil destruction that may occur in association withsome bacterial or viral infections, allergic disorders, autoimmunediseases, conditions in which an individual has an enlarged spleen(e.g., Felty syndrome, malaria and sarcoidosis), and some drug treatmentregimens.

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be useful indiagnosing, prognosing, preventing, and/or treating lymphocytopenias(decreased numbers of B and/or T lymphocytes), including, but notlimited to, lymphocytopenias resulting from or associated with stress,drug treatments (e.g., drug treatment with corticosteroids, cancerchemotherapies, and/or radiation therapies), AIDS infection and/or otherdiseases such as, for example, cancer, rheumatoid arthritis, systemiclupus erythematosus, chronic infections, some viral infections and/orhereditary disorders (e.g., DiGeorge syndrome, Wiskott-Aldrich Syndrome,severe combined immunodeficiency, ataxia telangiectsia).

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be useful indiagnosing, prognosing, preventing, and/or treating diseases anddisorders associated with macrophage numbers and/or macrophage functionincluding, but not limited to, Gaucher's disease, Niemann-Pick disease,Letterer-Siwe disease and Hand-Schuller-Christian disease.

In another embodiment, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in diagnosing, prognosing, preventing, and/or treatingdiseases and disorders associated with eosinophil numbers and/oreosinophil function including, but not limited to, idiopathichypereosinophilic syndrome, eosinophilia-myalgia syndrome, andHand-Schuller-Christian disease.

In yet another embodiment, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in diagnosing, prognosing, preventing, and/or treatingleukemias and lymphomas including, but not limited to, acute lymphocytic(lymphpblastic) leukemia (ALL), acute myeloid (myelocytic, myelogenous,myeloblastic, or myelomonocytic) leukemia, chronic lymphocytic leukemia(e.g., B cell leukemias, T cell leukemias, Sezary syndrome, and Hairycell leukemia), chronic myelocytic (myeloid, myelogenous, orgranulocytic) leukemia, Hodgkin's lymphoma, non-hodgkin's lymphoma,Burkitt's lymphoma, and mycosis fungoides.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in diagnosing, prognosing, preventing, and/or treatingdiseases and disorders of plasma cells including, but not limited to,plasma cell dyscrasias, monoclonal gammaopathies, monoclonalgammopathies of undetermined significance, multiple myeloma,macroglobulinemia, Waldenstrom's macroglobulinemia, cryoglobulinemia,and Raynaud's phenomenon.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in treating, preventing, and/or diagnosingmyeloproliferative disorders, including but not limited to, polycythemiavera, relative polycythemia, secondary polycythemia, myelofibrosis,acute myelofibrosis, agnogenic myelod metaplasia, thrombocythemia,(including both primary and secondary thrombocythemia) and chronicmyelocytic leukemia.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful as a treatment prior to surgery, to increase blood cellproduction.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful as an agent to enhance the migration, phagocytosis,superoxide production, antibody dependent cellular cytotoxicity ofneutrophils, eosionophils and macrophages.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful as an agent to increase the number of stem cells incirculation prior to stem cells pheresis. In another specificembodiment, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beuseful as an agent to increase the number of stem cells in circulationprior to platelet pheresis.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful as an agent to increase cytokine production.

In other embodiments, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful in preventing, diagnosing, and/or treating primaryhematopoietic disorders.

Hyperproliferative Disorders

In certain embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention can beused to treat or detect hyperproliferative disorders, includingneoplasms. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention mayinhibit the proliferation of the disorder through direct or indirectinteractions. Alternatively, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention mayproliferate other cells which can inhibit the hyperproliferativedisorder.

For example, by increasing an immune response, particularly increasingantigenic qualities of the hyperproliferative disorder or byproliferating, differentiating, or mobilizing T-cells,hyperproliferative disorders can be treated. This immune response may beincreased by either enhancing an existing immune response, or byinitiating a new immune response. Alternatively, decreasing an immuneresponse may also be a method of treating hyperproliferative disorders,such as a chemotherapeutic agent.

Examples of hyperproliferative disorders that can be treated or detectedby fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention include, but are not limited toneoplasms located in the: colon, abdomen, bone, breast, digestivesystem, liver, pancreas, peritoneum, endocrine glands (adrenal,parathyroid, pituitary, testicles, ovary, thymus, thyroid), eye, headand neck, nervous (central and peripheral), lymphatic system, pelvis,skin, soft tissue, spleen, thorax, and urogenital tract.

Similarly, other hyperproliferative disorders can also be treated ordetected by fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention. Examples of suchhyperproliferative disorders include, but are not limited to: AcuteChildhood Lymphoblastic Leukemia, Acute Lymphoblastic Leukemia, AcuteLymphocytic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma,Adult (Primary) Hepatocellular Cancer, Adult (Primary) Liver Cancer,Adult Acute Lymphocytic Leukemia, Adult Acute Myeloid Leukemia, AdultHodgkin's Disease, Adult Hodgkin's Lymphoma, Adult Lymphocytic Leukemia,Adult Non-Hodgkin's Lymphoma, Adult Primary Liver Cancer, Adult SoftTissue Sarcoma, AIDS-Related Lymphoma, AIDS-Related Malignancies, AnalCancer, Astrocytoma, Bile Duct Cancer, Bladder Cancer, Bone Cancer,Brain Stem Glioma, Brain Tumors, Breast Cancer, Cancer of the RenalPelvis and Ureter, Central Nervous System (Primary) Lymphoma, CentralNervous System Lymphoma, Cerebellar Astrocytoma, Cerebral Astrocytoma,Cervical Cancer, Childhood (Primary) Hepatocellular Cancer, Childhood(Primary) Liver Cancer, Childhood Acute Lymphoblastic Leukemia,Childhood Acute Myeloid Leukemia, Childhood Brain Stem Glioma, ChildhoodCerebellar Astrocytoma, Childhood Cerebral Astrocytoma, ChildhoodExtracranial Germ Cell Tumors, Childhood Hodgkin's Disease, ChildhoodHodgkin's Lymphoma, Childhood Hypothalamic and Visual Pathway Glioma,Childhood Lymphoblastic Leukemia, Childhood Medulloblastoma, ChildhoodNon-Hodgkin's Lymphoma, Childhood Pineal and Supratentorial PrimitiveNeuroectodermal Tumors, Childhood Primary Liver Cancer, ChildhoodRhabdomyosarcoma, Childhood Soft Tissue Sarcoma, Childhood VisualPathway and Hypothalamic Glioma, Chronic Lymphocytic Leukemia, ChronicMyelogenous Leukemia, Colon Cancer, Cutaneous T-Cell Lymphoma, EndocrinePancreas Islet Cell Carcinoma, Endometrial Cancer, Ependymoma,Epithelial Cancer, Esophageal Cancer, Ewing's Sarcoma and RelatedTumors, Exocrine Pancreatic Cancer, Extracranial Germ Cell Tumor,Extragonadal Germ Cell Tumor, Extrahepatic Bile Duct Cancer, Eye Cancer,Female Breast Cancer, Gaucher's Disease, Gallbladder Cancer, GastricCancer, Gastrointestinal Carcinoid Tumor, Gastrointestinal Tumors, GermCell Tumors, Gestational Trophoblastic Tumor, Hairy Cell Leukemia, Headand Neck Cancer, Hepatocellular Cancer, Hodgkin's Disease, Hodgkin'sLymphoma, Hypergammaglobulinemia, Hypopharyngeal Cancer, IntestinalCancers, Intraocular Melanoma, Islet Cell Carcinoma, Islet CellPancreatic Cancer, Kaposi's Sarcoma, Kidney Cancer, Laryngeal Cancer,Lip and Oral Cavity Cancer, Liver Cancer, Lung Cancer,Lymphoproliferative Disorders, Macroglobulinemia, Male Breast Cancer,Malignant Mesothelioma, Malignant Thymoma, Medulloblastoma, Melanoma,Mesothelioma, Metastatic Occult Primary Squamous Neck Cancer, MetastaticPrimary Squamous Neck Cancer, Metastatic Squamous Neck Cancer, MultipleMyeloma, Multiple Myeloma/Plasma Cell Neoplasm, MyelodysplasticSyndrome, Myelogenous Leukemia, Myeloid Leukemia, MyeloproliferativeDisorders, Nasal Cavity and Paranasal Sinus Cancer, NasopharyngealCancer, Neuroblastoma, Non-Hodgkin's Lymphoma During Pregnancy,Nonmelanoma Skin Cancer, Non-Small Cell Lung Cancer, Occult PrimaryMetastatic Squamous Neck Cancer, Oropharyngeal Cancer, Osteo-/MalignantFibrous Sarcoma, Osteosarcoma/Malignant Fibrous Histiocytoma,Osteosarcoma/Malignant Fibrous Histiocytoma of Bone, Ovarian EpithelialCancer, Ovarian Germ Cell Tumor, Ovarian Low Malignant Potential Tumor,Pancreatic Cancer, Paraproteinemias, Purpura, Parathyroid Cancer, PenileCancer, Pheochromocytoma, Pituitary Tumor, Plasma Cell Neoplasm/MultipleMyeloma, Primary Central Nervous System Lymphoma, Primary Liver Cancer,Prostate Cancer, Rectal Cancer, Renal Cell Cancer, Renal Pelvis andUreter Cancer, Retinoblastoma, Rhabdomyosarcoma, Salivary Gland Cancer,Sarcoidosis Sarcomas, Sezary Syndrome, Skin Cancer, Small Cell LungCancer, Small Intestine Cancer, Soft Tissue Sarcoma, Squamous NeckCancer, Stomach Cancer, Supratentorial Primitive Neuroectodermal andPineal Tumors, T-Cell Lymphoma, Testicular Cancer, Thymoma, ThyroidCancer, Transitional Cell Cancer of the Renal Pelvis and Ureter,Transitional Renal Pelvis and Ureter Cancer, Trophoblastic Tumors,Ureter and Renal Pelvis Cell Cancer, Urethral Cancer, Uterine Cancer,Uterine Sarcoma, Vaginal Cancer, Visual Pathway and Hypothalamic Glioma,Vulvar Cancer, Waldenstrom's Macroglobulinemia, Wilms' Tumor, and anyother hyperproliferative disease, besides neoplasia, located in an organsystem listed above.

In another preferred embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used to diagnose, prognose, prevent, and/or treatpremalignant conditions and to prevent progression to a neoplastic ormalignant state, including but not limited to those disorders describedabove. Such uses are indicated in conditions known or suspected ofpreceding progression to neoplasia or cancer, in particular, wherenon-neoplastic cell growth consisting of hyperplasia, metaplasia, ormost particularly, dysplasia has occurred (for review of such abnormalgrowth conditions, see Robbins and Angell, 1976, Basic Pathology, 2dEd., W. B. Saunders Co., Philadelphia, pp. 68-79.)

Hyperplasia is a form of controlled cell proliferation, involving anincrease in cell number in a tissue or organ, without significantalteration in structure or function. Hyperplastic disorders which can bediagnosed, prognosed, prevented, and/or treated with fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention include, but are not limited to, angiofollicularmediastinal lymph node hyperplasia, angiolymphoid hyperplasia witheosinophilia, atypical melanocytic hyperplasia, basal cell hyperplasia,benign giant lymph node hyperplasia, cementum hyperplasia, congenitaladrenal hyperplasia, congenital sebaceous hyperplasia, cystichyperplasia, cystic hyperplasia of the breast, denture hyperplasia,ductal hyperplasia, endometrial hyperplasia, fibromuscular hyperplasia,focal epithelial hyperplasia, gingival hyperplasia, inflammatory fibroushyperplasia, inflammatory papillary hyperplasia, intravascular papillaryendothelial hyperplasia, nodular hyperplasia of prostate, nodularregenerative hyperplasia, pseudoepitheliomatous hyperplasia, senilesebaceous hyperplasia, and verrucous hyperplasia.

Metaplasia is a form of controlled cell growth in which one type ofadult or fully differentiated cell substitutes for another type of adultcell. Metaplastic disorders which can be diagnosed, prognosed,prevented, and/or treated with fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventioninclude, but are not limited to, agnogenic myeloid metaplasia, apocrinemetaplasia, atypical metaplasia, autoparenchymatous metaplasia,connective tissue metaplasia, epithelial metaplasia, intestinalmetaplasia, metaplastic anemia, metaplastic ossification, metaplasticpolyps, myeloid metaplasia, primary myeloid metaplasia, secondarymyeloid metaplasia, squamous metaplasia, squamous metaplasia of amnion,and symptomatic myeloid metaplasia.

Dysplasia is frequently a forerunner of cancer, and is found mainly inthe epithelia; it is the most disorderly form of non-neoplastic cellgrowth, involving a loss in individual cell uniformity and in thearchitectural orientation of cells. Dysplastic cells often haveabnormally large, deeply stained nuclei, and exhibit pleomorphism.Dysplasia characteristically occurs where there exists chronicirritation or inflammation. Dysplastic disorders which can be diagnosed,prognosed, prevented, and/or treated with fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention include, but are not limited to, anhidrotic ectodermaldysplasia, anterofacial dysplasia, asphyxiating thoracic dysplasia,atriodigital dysplasia, bronchopulmonary dysplasia, cerebral dysplasia,cervical dysplasia, chondroectodermal dysplasia, cleidocranialdysplasia, congenital ectodermal dysplasia, craniodiaphysial dysplasia,craniocarpotarsal dysplasia, craniometaphysial dysplasia, dentindysplasia, diaphysial dysplasia, ectodermal dysplasia, enamel dysplasia,encephalo-ophthalmic dysplasia, dysplasia epiphysialis hemimelia,dysplasia epiphysialis multiplex, dysplasia epiphysialis punctata,epithelial dysplasia, faciodigitogenital dysplasia, familial fibrousdysplasia of jaws, familial white folded dysplasia, fibromusculardysplasia, fibrous dysplasia of bone, florid osseous dysplasia,hereditary renal-retinal dysplasia, hidrotic ectodermal dysplasia,hypohidrotic ectodermal dysplasia, lymphopenic thymic dysplasia, mammarydysplasia, mandibulofacial dysplasia, metaphysial dysplasia, Mondinidysplasia, monostotic fibrous dysplasia, mucoepithelial dysplasia,multiple epiphysial dysplasia, oculoauriculovertebral dysplasia,oculodentodigital dysplasia, oculovertebral dysplasia, odontogenicdysplasia, ophthalmomandibulomelic dysplasia, periapical cementaldysplasia, polyostotic fibrous dysplasia, pseudoachondroplasticspondyloepiphysial dysplasia, retinal dysplasia, septo-optic dysplasia,spondyloepiphysial dysplasia, and ventriculoradial dysplasia.

Additional pre-neoplastic disorders which can be diagnosed, prognosed,prevented, and/or treated with fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventioninclude, but are not limited to, benign dysproliferative disorders(e.g., benign tumors, fibrocystic conditions, tissue hypertrophy,intestinal polyps, colon polyps, and esophageal dysplasia), leukoplakia,keratoses, Bowen's disease, Farmer's Skin, solar cheilitis, and solarkeratosis.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, maybe used to diagnose and/or prognose disorders associated with thetissue(s) in which the polypeptide of the invention is expressed.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventionconjugated to a toxin or a radioactive isotope, as described herein, maybe used to treat cancers and neoplasms, including, but not limited to,those described herein. In a further preferred embodiment, albuminfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention conjugated to a toxin or a radioactiveisotope, as described herein, may be used to treat acute myelogenousleukemia.

Additionally, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may affect apoptosis,and therefore, would be useful in treating a number of diseasesassociated with increased cell survival or the inhibition of apoptosis.For example, diseases associated with increased cell survival or theinhibition of apoptosis that could be diagnosed, prognosed, prevented,and/or treated by polynucleotides, polypeptides, and/or agonists orantagonists of the invention, include cancers (such as follicularlymphomas, carcinomas with p53 mutations, and hormone-dependent tumors,including, but not limited to colon cancer, cardiac tumors, pancreaticcancer, melanoma, retinoblastoma, glioblastoma, lung cancer, intestinalcancer, testicular cancer, stomach cancer, neuroblastoma, myxoma, myoma,lymphoma, endothelioma, osteoblastoma, osteoclastoma, osteosarcoma,chondrosarcoma, adenoma, breast cancer, prostate cancer, Kaposi'ssarcoma and ovarian cancer); autoimmune disorders such as, multiplesclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliarycirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemiclupus erythematosus and immune-related glomerulonephritis and rheumatoidarthritis) and viral infections (such as herpes viruses, pox viruses andadenoviruses), inflammation, graft v. host disease, acute graftrejection, and chronic graft rejection.

In preferred embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to inhibit growth, progression, and/or metastasis of cancers, inparticular those listed above.

Additional diseases or conditions associated with increased cellsurvival that could be diagnosed, prognosed, prevented, and/or treatedby fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, include, but are not limitedto, progression, and/or metastases of malignancies and related disorderssuch as leukemia (including acute leukemias (e.g., acute lymphocyticleukemia, acute myelocytic leukemia (including myeloblastic,promyelocytic, myelomonocytic, monocytic, and erythroleukemia)) andchronic leukemias (e.g., chronic myelocytic (granulocytic) leukemia andchronic lymphocytic leukemia)), polycythemia vera, lymphomas (e.g.,Hodgkin's disease and non-Hodgkin's disease), multiple myeloma,Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumorsincluding, but not limited to, sarcomas and carcinomas such asfibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenicsarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma,lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor,leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer,breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma,basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceousgland carcinoma, papillary carcinoma, papillary adenocarcinomas,cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renalcell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma,seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testiculartumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma,epithelial carcinoma, glioma, astrocytoma, medulloblastoma,craniopharyngioma, ependymoma, pinealoma, emangioblastoma, acousticneuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, andretinoblastoma.

Diseases associated with increased apoptosis that could be diagnosed,prognosed, prevented, and/or treated by fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention, include AIDS; neurodegenerative disorders (such asAlzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis,retinitis pigmentosa, cerebellar degeneration and brain tumor or priorassociated disease); autoimmune disorders (such as, multiple sclerosis,Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet'sdisease, Crohn's disease, polymyositis, systemic lupus erythematosus andimmune-related glomerulonephritis and rheumatoid arthritis)myelodysplastic syndromes (such as aplastic anemia), graft v. hostdisease, ischemic injury (such as that caused by myocardial infarction,stroke and reperfusion injury), liver injury (e.g., hepatitis relatedliver injury, ischemia/reperfusion injury, cholestosis (bile ductinjury) and liver cancer); toxin-induced liver disease (such as thatcaused by alcohol), septic shock, cachexia and anorexia.

Hyperproliferative diseases and/or disorders that could be diagnosed,prognosed, prevented, and/or treated by fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention, include, but are not limited to, neoplasms located in theliver, abdomen, bone, breast, digestive system, pancreas, peritoneum,endocrine glands (adrenal, parathyroid, pituitary, testicles, ovary,thymus, thyroid), eye, head and neck, nervous system (central andperipheral), lymphatic system, pelvis, skin, soft tissue, spleen,thorax, and urogenital tract.

Similarly, other hyperproliferative disorders can also be diagnosed,prognosed, prevented, and/or treated by fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention. Examples of such hyperproliferative disorders include, butare not limited to: hypergammaglobulinemia, lymphoproliferativedisorders, paraproteinemias, purpura, sarcoidosis, Sezary Syndrome,Waldenstron's macroglobulinemia, Gaucher's Disease, histiocytosis, andany other hyperproliferative disease, besides neoplasia, located in anorgan system listed above.

Another preferred embodiment utilizes polynucleotides encoding albuminfusion proteins of the invention to inhibit aberrant cellular division,by gene therapy using the present invention, and/or protein fusions orfragments thereof.

Thus, the present invention provides a method for treating cellproliferative disorders by inserting into an abnormally proliferatingcell a polynucleotide encoding an albumin fusion protein of the presentinvention, wherein said polynucleotide represses said expression.

Another embodiment of the present invention provides a method oftreating cell-proliferative disorders in individuals comprisingadministration of one or more active gene copies of the presentinvention to an abnormally proliferating cell or cells. In a preferredembodiment, polynucleotides of the present invention is a DNA constructcomprising a recombinant expression vector effective in expressing a DNAsequence encoding said polynucleotides. In another preferred embodimentof the present invention, the DNA construct encoding the fusion proteinof the present invention is inserted into cells to be treated utilizinga retrovirus, or more preferably an adenoviral vector (See G J. Nabel,et. al., PNAS 1999 96: 324-326, which is hereby incorporated byreference). In a most preferred embodiment, the viral vector isdefective and will not transform non-proliferating cells, onlyproliferating cells. Moreover, in a preferred embodiment, thepolynucleotides of the present invention inserted into proliferatingcells either alone, or in combination with or fused to otherpolynucleotides, can then be modulated via an external stimulus (i.e.magnetic, specific small molecule, chemical, or drug administration,etc.), which acts upon the promoter upstream of said polynucleotides toinduce expression of the encoded protein product. As such the beneficialtherapeutic affect of the present invention may be expressly modulated(i.e. to increase, decrease, or inhibit expression of the presentinvention) based upon said external stimulus.

Polynucleotides of the present invention may be useful in repressingexpression of oncogenic genes or antigens. By “repressing expression ofthe oncogenic genes” is intended the suppression of the transcription ofthe gene, the degradation of the gene transcript (pre-message RNA), theinhibition of splicing, the destruction of the messenger RNA, theprevention of the post-translational modifications of the protein, thedestruction of the protein, or the inhibition of the normal function ofthe protein.

For local administration to abnormally proliferating cells,polynucleotides of the present invention may be administered by anymethod known to those of skill in the art including, but not limited totransfection, electroporation, microinjection of cells, or in vehiclessuch as liposomes, lipofectin, or as naked polynucleotides, or any othermethod described throughout the specification. The polynucleotide of thepresent invention may be delivered by known gene delivery systems suchas, but not limited to, retroviral vectors (Gilboa, J. Virology 44:845(1982); Hocke, Nature 320:275 (1986); Wilson, et al., Proc. Natl. Acad.Sci. U.S.A. 85:3014), vaccinia virus system (Chakrabarty et al., Mol.Cell Biol. 5:3403 (1985) or other efficient DNA delivery systems (Yateset al., Nature 313:812 (1985)) known to those skilled in the art. Thesereferences are exemplary only and are hereby incorporated by reference.In order to specifically deliver or transfect cells which are abnormallyproliferating and spare non-dividing cells, it is preferable to utilizea retrovirus, or adenoviral (as described in the art and elsewhereherein) delivery system known to those of skill in the art. Since hostDNA replication is required for retroviral DNA to integrate and theretrovirus will be unable to self replicate due to the lack of theretrovirus genes needed for its life cycle. Utilizing such a retroviraldelivery system for polynucleotides of the present invention will targetsaid gene and constructs to abnormally proliferating cells and willspare the non-dividing normal cells.

The polynucleotides of the present invention may be delivered directlyto cell proliferative disorder/disease sites in internal organs, bodycavities and the like by use of imaging devices used to guide aninjecting needle directly to the disease site. The polynucleotides ofthe present invention may also be administered to disease sites at thetime of surgical intervention.

By “cell proliferative disease” is meant any human or animal disease ordisorder, affecting any one or any combination of organs, cavities, orbody parts, which is characterized by single or multiple local abnormalproliferations of cells, groups of cells, or tissues, whether benign ormalignant.

Any amount of the polynucleotides of the present invention may beadministered as long as it has a biologically inhibiting effect on theproliferation of the treated cells. Moreover, it is possible toadminister more than one of the polynucleotide of the present inventionsimultaneously to the same site. By “biologically inhibiting” is meantpartial or total growth inhibition as well as decreases in the rate ofproliferation or growth of the cells. The biologically inhibitory dosemay be determined by assessing the effects of the polynucleotides of thepresent invention on target malignant or abnormally proliferating cellgrowth in tissue culture, tumor growth in animals and cell cultures, orany other method known to one of ordinary skill in the art.

Moreover, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention of the presentinvention are useful in inhibiting the angiogenesis of proliferativecells or tissues, either alone, as a protein fusion, or in combinationwith other polypeptides directly or indirectly, as described elsewhereherein. In a most preferred embodiment, said anti-angiogenesis effectmay be achieved indirectly, for example, through the inhibition ofhematopoietic, tumor-specific cells, such as tumor-associatedmacrophages (See Joseph I B, et al. J Natl Cancer Inst, 90(21):1648-53(1998), which is hereby incorporated by reference).

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in inhibitingproliferative cells or tissues through the induction of apoptosis. Thesefusion proteins and/or polynucleotides may act either directly, orindirectly to induce apoptosis of proliferative cells and tissues, forexample in the activation of a death-domain receptor, such as tumornecrosis factor (TNF) receptor-1, CD95 (Fas/APO-1), TNF-receptor-relatedapoptosis-mediated protein (TRAMP) and TNF-related apoptosis-inducingligand (TRAIL) receptor-1 and -2 (See Schulze-Osthoff K, et. al., Eur JBiochem 254(3):439-59 (1998), which is hereby incorporated byreference). Moreover, in another preferred embodiment of the presentinvention, these fusion proteins and/or polynucleotides may induceapoptosis through other mechanisms, such as in the activation of otherproteins which will activate apoptosis, or through stimulating theexpression of these proteins, either alone or in combination with smallmolecule drugs or adjuvants, such as apoptonin, galectins, thioredoxins,anti-inflammatory proteins (See for example, Mutat Res 400(1-2):447-55(1998), Med Hypotheses. 50(5):423-33 (1998), Chem Biol Interact. April24; 111-112:23-34 (1998), J Mol Med. 76(6):402-12 (1998), Int J TissueReact; 20(1):3-15 (1998), which are all hereby incorporated byreference).

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention are useful in inhibiting themetastasis of proliferative cells or tissues. Inhibition may occur as adirect result of administering these albumin fusion proteins and/orpolynucleotides, or indirectly, such as activating the expression ofproteins known to inhibit metastasis, for example alpha 4 integrins,(See, e.g., Curr Top Microbiol Immunol 1998; 231:125-41, which is herebyincorporated by reference). Such therapeutic affects of the presentinvention may be achieved either alone, or in combination with smallmolecule drugs or adjuvants.

In another embodiment, the invention provides a method of deliveringcompositions containing the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionto targeted cells expressing the a polypeptide bound by, that binds to,or associates with an albumin fusion protein of the invention. Albuminfusion proteins of the invention may be associated with heterologouspolypeptides, heterologous nucleic acids, toxins, or prodrugs viahydrophobic, hydrophilic, ionic and/or covalent interactions.

Albumin fusion proteins of the invention are useful in enhancing theimmunogenicity and/or antigenicity of proliferating cells or tissues,either directly, such as would occur if the albumin fusion proteins ofthe invention ‘vaccinated’ the immune response to respond toproliferative antigens and immunogens, or indirectly, such as inactivating the expression of proteins known to enhance the immuneresponse (e.g. chemokines), to said antigens and immunogens.

Renal Disorders

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, may be used to treat, prevent,diagnose, and/or prognose disorders of the renal system. Renal disorderswhich can be diagnosed, prognosed, prevented, and/or treated withcompositions of the invention include, but are not limited to, kidneyfailure, nephritis, blood vessel disorders of kidney, metabolic andcongenital kidney disorders, urinary disorders of the kidney, autoimmunedisorders, sclerosis and necrosis, electrolyte imbalance, and kidneycancers.

Kidney diseases which can be diagnosed, prognosed, prevented, and/ortreated with compositions of the invention include, but are not limitedto, acute kidney failure, chronic kidney failure, atheroembolic renalfailure, end-stage renal disease, inflammatory diseases of the kidney(e.g., acute glomerulonephritis, postinfectious glomerulonephritis,rapidly progressive glomerulonephritis, nephrotic syndrome, membranousglomerulonephritis, familial nephrotic syndrome, membranoproliferativeglomerulonephritis I and II, mesangial proliferative glomerulonephritis,chronic glomerulonephritis, acute tubulointerstitial nephritis, chronictubulointerstitial nephritis, acute post-streptococcalglomerulonephritis (PSGN), pyelonephritis, lupus nephritis, chronicnephritis, interstitial nephritis, and post-streptococcalglomerulonephritis), blood vessel disorders of the kidneys (e.g., kidneyinfarction, atheroembolic kidney disease, cortical necrosis, malignantnephrosclerosis, renal vein thrombosis, renal underperfusion, renalretinopathy, renal ischemia-reperfusion, renal artery embolism, andrenal artery stenosis), and kidney disorders resulting form urinarytract disease (e.g., pyelonephritis, hydronephrosis, urolithiasis (renallithiasis, nephrolithiasis), reflux nephropathy, urinary tractinfections, urinary retention, and acute or chronic unilateralobstructive uropathy.)

In addition, compositions of the invention can be used to diagnose,prognose, prevent, and/or treat metabolic and congenital disorders ofthe kidney (e.g., uremia, renal amyloidosis, renal osteodystrophy, renaltubular acidosis, renal glycosuria, nephrogenic diabetes insipidus,cystinuria, Fanconi's syndrome, renal fibrocystic osteosis (renalrickets), Hartnup disease, Bartter's syndrome, Liddle's syndrome,polycystic kidney disease, medullary cystic disease, medullary spongekidney, Alport's syndrome, nail-patella syndrome, congenital nephroticsyndrome, CRUSH syndrome, horseshoe kidney, diabetic nephropathy,nephrogenic diabetes insipidus, analgesic nephropathy, kidney stones,and membranous nephropathy), and autoimmune disorders of the kidney(e.g., systemic lupus erythematosus (SLE), Goodpasture syndrome, IgAnephropathy, and IgM mesangial proliferative glomerulonephritis).

Compositions of the invention can also be used to diagnose, prognose,prevent, and/or treat sclerotic or necrotic disorders of the kidney(e.g., glomerulosclerosis, diabetic nephropathy, focal segmentalglomerulosclerosis (FSGS), necrotizing glomerulonephritis, and renalpapillary necrosis), cancers of the kidney (e.g., nephroma,hypernephroma, nephroblastoma, renal cell cancer, transitional cellcancer, renal adenocarcinoma, squamous cell cancer, and Wilm's tumor),and electrolyte imbalances (e.g., nephrocalcinosis, pyuria, edema,hydronephritis, proteinuria, hyponatremia, hypernatremia, hypokalemia,hyperkalemia, hypocalcemia, hypercalcemia, hypophosphatemia, andhyperphosphatemia).

Compositions of the invention may be administered using any method knownin the art, including, but not limited to, direct needle injection atthe delivery site, intravenous injection, topical administration,catheter infusion, biolistic injectors, particle accelerators, gelfoamsponge depots, other commercially available depot materials, osmoticpumps, oral or suppositorial solid pharmaceutical formulations,decanting or topical applications during surgery, aerosol delivery. Suchmethods are known in the art. Compositions of the invention may beadministered as part of a Therapeutic, described in more detail below.Methods of delivering polynucleotides of the invention are described inmore detail herein.

Cardiovascular Disorders

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, may be used to treat, prevent,diagnose, and/or prognose cardiovascular disorders, including, but notlimited to, peripheral artery disease, such as limb ischemia.

Cardiovascular disorders include, but are not limited to, cardiovascularabnormalities, such as arterio-arterial fistula, arteriovenous fistula,cerebral arteriovenous malformations, congenital heart defects,pulmonary atresia, and Scimitar Syndrome. Congenital heart defectsinclude, but are not limited to, aortic coarctation, cor triatriatum,coronary vessel anomalies, crisscross heart, dextrocardia, patent ductusarteriosus, Ebstein's anomaly, Eisenmenger complex, hypoplastic leftheart syndrome, levocardia, tetralogy of fallot, transposition of greatvessels, double outlet right ventricle, tricuspid atresia, persistenttruncus arteriosus, and heart septal defects, such as aortopulmonaryseptal defect, endocardial cushion defects, Lutembacher's Syndrome,trilogy of Fallot, ventricular heart septal defects.

Cardiovascular disorders also include, but are not limited to, heartdisease, such as arrhythmias, carcinoid heart disease, high cardiacoutput, low cardiac output, cardiac tamponade, endocarditis (includingbacterial), heart aneurysm, cardiac arrest, congestive heart failure,congestive cardiomyopathy, paroxysmal dyspnea, cardiac edema, hearthypertrophy, congestive cardiomyopathy, left ventricular hypertrophy,right ventricular hypertrophy, post-infarction heart rupture,ventricular septal rupture, heart valve diseases, myocardial diseases,myocardial ischemia, pericardial effusion, pericarditis (includingconstrictive and tuberculous), pneumopericardium, postpericardiotomysyndrome, pulmonary heart disease, rheumatic heart disease, ventriculardysfunction, hyperemia, cardiovascular pregnancy complications, ScimitarSyndrome, cardiovascular syphilis, and cardiovascular tuberculosis.

Arrhythmias include, but are not limited to, sinus arrhythmia, atrialfibrillation, atrial flutter, bradycardia, extrasystole, Adams-StokesSyndrome, bundle-branch block, sinoatrial block, long QT syndrome,parasystole, Lown-Ganong-Levine Syndrome, Mahaim-type pre-excitationsyndrome, Wolff-Parkinson-White syndrome, sick sinus syndrome,tachycardias, and ventricular fibrillation. Tachycardias includeparoxysmal tachycardia, supraventricular tachycardia, acceleratedidioventricular rhythm, atrioventricular nodal reentry tachycardia,ectopic atrial tachycardia, ectopic junctional tachycardia, sinoatrialnodal reentry tachycardia, sinus tachycardia, Torsades de Pointes, andventricular tachycardia.

Heart valve diseases include, but are not limited to, aortic valveinsufficiency, aortic valve stenosis, hear murmurs, aortic valveprolapse, mitral valve prolapse, tricuspid valve prolapse, mitral valveinsufficiency, mitral valve stenosis, pulmonary atresia, pulmonary valveinsufficiency, pulmonary valve stenosis, tricuspid atresia, tricuspidvalve insufficiency, and tricuspid valve stenosis.

Myocardial diseases include, but are not limited to, alcoholiccardiomyopathy, congestive cardiomyopathy, hypertrophic cardiomyopathy,aortic subvalvular stenosis, pulmonary subvalvular stenosis, restrictivecardiomyopathy, Chagas cardiomyopathy, endocardial fibroelastosis,endomyocardial fibrosis, Kearns Syndrome, myocardial reperfusion injury,and myocarditis.

Myocardial ischemias include, but are not limited to, coronary disease,such as angina pectoris, coronary aneurysm, coronary arteriosclerosis,coronary thrombosis, coronary vasospasm, myocardial infarction andmyocardial stunning.

Cardiovascular diseases also include vascular diseases such asaneurysms, angiodysplasia, angiomatosis, bacillary angiomatosis,Hippel-Lindau Disease, Klippel-Trenaunay-Weber Syndrome, Sturge-WeberSyndrome, angioneurotic edema, aortic diseases, Takayasu's Arteritis,aortitis, Leriche's Syndrome, arterial occlusive diseases, arteritis,enarteritis, polyarteritis nodosa, cerebrovascular disorders, diabeticangiopathies, diabetic retinopathy, embolisms, thrombosis,erythromelalgia, hemorrhoids, hepatic veno-occlusive disease,hypertension, hypotension, ischemia, peripheral vascular diseases,phlebitis, pulmonary veno-occlusive disease, Raynaud's disease, CRESTsyndrome, retinal vein occlusion, Scimitar syndrome, superior vena cavasyndrome, telangiectasia, atacia telangiectasia, hereditary hemorrhagictelangiectasia, varicocele, varicose veins, varicose ulcer, vasculitis,and venous insufficiency.

Aneurysms include, but are not limited to, dissecting aneurysms, falseaneurysms, infected aneurysms, ruptured aneurysms, aortic aneurysms,cerebral aneurysms, coronary aneurysms, heart aneurysms, and iliacaneurysms.

Arterial occlusive diseases include, but are not limited to,arteriosclerosis, intermittent claudication, carotid stenosis,fibromuscular dysplasias, mesenteric vascular occlusion, Moyamoyadisease, renal artery obstruction, retinal artery occlusion, andthromboangiitis obliterans.

Cerebrovascular disorders include, but are not limited to, carotidartery diseases, cerebral amyloid angiopathy, cerebral aneurysm,cerebral anoxia, cerebral arteriosclerosis, cerebral arteriovenousmalformation, cerebral artery diseases, cerebral embolism andthrombosis, carotid artery thrombosis, sinus thrombosis, Wallenberg'ssyndrome, cerebral hemorrhage, epidural hematoma, subdural hematoma,subaraxhnoid hemorrhage, cerebral infarction, cerebral ischemia(including transient), subclavian steal syndrome, periventricularleukomalacia, vascular headache, cluster headache, migraine, andvertebrobasilar insufficiency.

Embolisms include, but are not limited to, air embolisms, amniotic fluidembolisms, cholesterol embolisms, blue toe syndrome, fat embolisms,pulmonary embolisms, and thromoboembolisms. Thrombosis include, but arenot limited to, coronary thrombosis, hepatic vein thrombosis, retinalvein occlusion, carotid artery thrombosis, sinus thrombosis,Wallenberg's syndrome, and thrombophlebitis.

Ischemic disorders include, but are not limited to, cerebral ischemia,ischemic colitis, compartment syndromes, anterior compartment syndrome,myocardial ischemia, reperfusion injuries, and peripheral limb ischemia.Vasculitis includes, but is not limited to, aortitis, arteritis,Behcet's Syndrome, Churg-Strauss Syndrome, mucocutaneous lymph nodesyndrome, thromboangiitis obliterans, hypersensitivity vasculitis,Schoenlein-Henoch purpura, allergic cutaneous vasculitis, and Wegener'sgranulomatosis.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be administered using anymethod known in the art, including, but not limited to, direct needleinjection at the delivery site, intravenous injection, topicaladministration, catheter infusion, biolistic injectors, particleaccelerators, gelfoam sponge depots, other commercially available depotmaterials, osmotic pumps, oral or suppositorial solid pharmaceuticalformulations, decanting or topical applications during surgery, aerosoldelivery. Such methods are known in the art. Methods of deliveringpolynucleotides are described in more detail herein.

Respiratory Disorders

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be used to treat, prevent,diagnose, and/or prognose diseases and/or disorders of the respiratorysystem.

Diseases and disorders of the respiratory system include, but are notlimited to, nasal vestibulitis, nonallergic rhinitis (e.g., acuterhinitis, chronic rhinitis, atrophic rhinitis, vasomotor rhinitis),nasal polyps, and sinusitis, juvenile angiofibromas, cancer of the noseand juvenile papillomas, vocal cord polyps, nodules (singer's nodules),contact ulcers, vocal cord paralysis, laryngoceles, pharyngitis (e.g.,viral and bacterial), tonsillitis, tonsillar cellulitis, parapharyngealabscess, laryngitis, laryngoceles, and throat cancers (e.g., cancer ofthe nasopharynx, tonsil cancer, larynx cancer), lung cancer (e.g.,squamous cell carcinoma, small cell (oat cell) carcinoma, large cellcarcinoma, and adenocarcinoma), allergic disorders (eosinophilicpneumonia, hypersensitivity pneumonitis (e.g., extrinsic allergicalveolitis, allergic interstitial pneumonitis, organic dustpneumoconiosis, allergic bronchopulmonary aspergillosis, asthma,Wegener's granulomatosis (granulomatous vasculitis), Goodpasture'ssyndrome)), pneumonia (e.g., bacterial pneumonia (e.g., Streptococcuspneumoniae (pneumoncoccal pneumonia), Staphylococcus aureus(staphylococcal pneumonia), Gram-negative bacterial pneumonia (causedby, e.g., Klebsiella and Pseudomas spp.), Mycoplasma pneumoniaepneumonia, Hemophilus influenzae pneumonia, Legionella pneumophila(Legionnaires' disease), and Chlamydia psittaci (Psittacosis)), andviral pneumonia (e.g., influenza, chickenpox (varicella).

Additional diseases and disorders of the respiratory system include, butare not limited to bronchiolitis, polio (poliomyelitis), croup,respiratory syncytial viral infection, mumps, erythema infectiosum(fifth disease), roseola infantum, progressive rubella panencephalitis,german measles, and subacute sclerosing panencephalitis), fungalpneumonia (e.g., Histoplasmosis, Coccidioidomycosis, Blastomycosis,fungal infections in people with severely suppressed immune systems(e.g., cryptococcosis, caused by Cryptococcus neoformans; aspergillosis,caused by Aspergillus spp.; candidiasis, caused by Candida; andmucormycosis)), Pneumocystis carinii (pneumocystis pneumonia), atypicalpneumonias (e.g., Mycoplasma and Chlamydia spp.), opportunisticinfection pneumonia, nosocomial pneumonia, chemical pneumonitis, andaspiration pneumonia, pleural disorders (e.g., pleurisy, pleuraleffusion, and pneumothorax (e.g., simple spontaneous pneumothorax,complicated spontaneous pneumothorax, tension pneumothorax)),obstructive airway diseases (e.g., asthma, chronic obstructive pulmonarydisease (COPD), emphysema, chronic or acute bronchitis), occupationallung diseases (e.g., silicosis, black lung (coal workers'pneumoconiosis), asbestosis, berylliosis, occupational asthma,byssinosis, and benign pneumoconioses), Infiltrative Lung Disease (e.g.,pulmonary fibrosis (e.g., fibrosing alveolitis, usual interstitialpneumonia), idiopathic pulmonary fibrosis, desquamative interstitialpneumonia, lymphoid interstitial pneumonia, histiocytosis X (e.g.,Letterer-Siwe disease, Hand-Schuller-Christian disease, eosinophilicgranuloma), idiopathic pulmonary hemosiderosis, sarcoidosis andpulmonary alveolar proteinosis), Acute respiratory distress syndrome(also called, e.g., adult respiratory distress syndrome), edema,pulmonary embolism, bronchitis (e.g., viral, bacterial), bronchiectasis,atelectasis, lung abscess (caused by, e.g., Staphylococcus aureus orLegionella pneumophila), and cystic fibrosis.

Anti-Angiogenesis Activity

The naturally occurring balance between endogenous stimulators andinhibitors of angiogenesis is one in which inhibitory influencespredominate. Rastinejad et al., Cell 56:345-355 (1989). In those rareinstances in which neovascularization occurs under normal physiologicalconditions, such as wound healing, organ regeneration, embryonicdevelopment, and female reproductive processes, angiogenesis isstringently regulated and spatially and temporally delimited. Underconditions of pathological angiogenesis such as that characterizingsolid tumor growth, these regulatory controls fail. Unregulatedangiogenesis becomes pathologic and sustains progression of manyneoplastic and non-neoplastic diseases. A number of serious diseases aredominated by abnormal neovascularization including solid tumor growthand metastases, arthritis, some types of eye disorders, and psoriasis.See, e.g., reviews by Moses et al., Biotech. 9:630-634 (1991); Folkmanet al., N. Engl. J. Med., 333:1757-1763 (1995); Auerbach et al., J.Microvasc. Res. 29:401-411 (1985); Folkman, Advances in Cancer Research,eds. Klein and Weinhouse, Academic Press, New York, pp. 175-203 (1985);Patz, Am. J. Opthalmol. 94:715-743 (1982); and Folkman et al., Science221:719-725 (1983). In a number of pathological conditions, the processof angiogenesis contributes to the disease state. For example,significant data have accumulated which suggest that the growth of solidtumors is dependent on angiogenesis. Folkman and Klagsbrun, Science235:442-447 (1987).

The present invention provides for treatment of diseases or disordersassociated with neovascularization by administration of fusion proteinsof the invention and/or polynucleotides encoding albumin fusion proteinsof the invention. Malignant and metastatic conditions which can betreated with the polynucleotides and polypeptides, or agonists orantagonists of the invention include, but are not limited to,malignancies, solid tumors, and cancers described herein and otherwiseknown in the art (for a review of such disorders, see Fishman et al.,Medicine, 2d Ed., J. B. Lippincott Co., Philadelphia (1985)).Thus, thepresent invention provides a method of treating an angiogenesis-relateddisease and/or disorder, comprising administering to an individual inneed thereof a therapeutically effective amount of an albumin fusionprotein of the invention and/or polynucleotides encoding an albuminfusion protein of the invention. For example, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may be utilized in a variety of additional methods in order totherapeutically treat a cancer or tumor. Cancers which may be treatedwith fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention include, but are not limited tosolid tumors, including prostate, lung, breast, ovarian, stomach,pancreas, larynx, esophagus, testes, liver, parotid, biliary tract,colon, rectum, cervix, uterus, endometrium, kidney, bladder, thyroidcancer; primary tumors and metastases; melanomas; glioblastoma; Kaposi'ssarcoma; leiomyosarcoma; non-small cell lung cancer; colorectal cancer;advanced malignancies; and blood born tumors such as leukemias. Forexample, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be deliveredtopically, in order to treat cancers such as skin cancer, head and necktumors, breast tumors, and Kaposi's sarcoma.

Within yet other aspects, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beutilized to treat superficial forms of bladder cancer by, for example,intravesical administration. Albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be delivered directly into the tumor, or near the tumor site, viainjection or a catheter. Of course, as the artisan of ordinary skillwill appreciate, the appropriate mode of administration will varyaccording to the cancer to be treated. Other modes of delivery arediscussed herein.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be useful in treating otherdisorders, besides cancers, which involve angiogenesis. These disordersinclude, but are not limited to: benign tumors, for example hemangiomas,acoustic neuromas, neurofibromas, trachomas, and pyogenic granulomas;artheroscleric plaques; ocular angiogenic diseases, for example,diabetic retinopathy, retinopathy of prematurity, macular degeneration,corneal graft rejection, neovascular glaucoma, retrolental fibroplasia,rubeosis, retinoblastoma, uvietis and Pterygia (abnormal blood vesselgrowth) of the eye; rheumatoid arthritis; psoriasis; delayed woundhealing; endometriosis; vasculogenesis; granulations; hypertrophic scars(keloids); nonunion fractures; scleroderma; trachoma; vascularadhesions; myocardial angiogenesis; coronary collaterals; cerebralcollaterals; arteriovenous malformations; ischemic limb angiogenesis;Osler-Webber Syndrome; plaque neovascularization; telangiectasia;hemophiliac joints; angiofibroma; fibromuscular dysplasia; woundgranulation; Crohn's disease; and atherosclerosis.

For example, within one aspect of the present invention methods areprovided for treating hypertrophic scars and keloids, comprising thestep of administering albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention to ahypertrophic scar or keloid.

Within one embodiment of the present invention fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are directly injected into a hypertrophic scar or keloid, inorder to prevent the progression of these lesions. This therapy is ofparticular value in the prophylactic treatment of conditions which areknown to result in the development of hypertrophic scars and keloids(e.g., burns), and is preferably initiated after the proliferative phasehas had time to progress (approximately 14 days after the initialinjury), but before hypertrophic scar or keloid development. As notedabove, the present invention also provides methods for treatingneovascular diseases of the eye, including for example, cornealneovascularization, neovascular glaucoma, proliferative diabeticretinopathy, retrolental fibroplasia and macular degeneration.

Moreover, Ocular disorders associated with neovascularization which canbe treated with the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the inventioninclude, but are not limited to: neovascular glaucoma, diabeticretinopathy, retinoblastoma, retrolental fibroplasia, uveitis,retinopathy of prematurity macular degeneration, corneal graftneovascularization, as well as other eye inflammatory diseases, oculartumors and diseases associated with choroidal or irisneovascularization. See, e.g., reviews by Waltman et al., Am. J.Ophthal. 85:704-710 (1978) and Gartner et al., Surv. Ophthal. 22:291-312(1978).

Thus, within one aspect of the present invention methods are providedfor treating neovascular diseases of the eye such as cornealneovascularization (including corneal graft neovascularization),comprising the step of administering to a patient a therapeuticallyeffective amount of a compound (e.g., fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention) to the cornea, such that the formation of blood vessels isinhibited. Briefly, the cornea is a tissue which normally lacks bloodvessels. In certain pathological conditions however, capillaries mayextend into the cornea from the pericorneal vascular plexus of thelimbus. When the cornea becomes vascularized, it also becomes clouded,resulting in a decline in the patient's visual acuity. Visual loss maybecome complete if the cornea completely opacitates. A wide variety ofdisorders can result in corneal neovascularization, including forexample, corneal infections (e.g., trachoma, herpes simplex keratitis,leishmaniasis and onchocerciasis), immunological processes (e.g., graftrejection and Stevens-Johnson's syndrome), alkali burns, trauma,inflammation (of any cause), toxic and nutritional deficiency states,and as a complication of wearing contact lenses.

Within particularly preferred embodiments of the invention, may beprepared for topical administration in saline (combined with any of thepreservatives and antimicrobial agents commonly used in ocularpreparations), and administered in eyedrop form. The solution orsuspension may be prepared in its pure form and administered severaltimes daily. Alternatively, anti-angiogenic compositions, prepared asdescribed above, may also be administered directly to the cornea. Withinpreferred embodiments, the anti-angiogenic composition is prepared witha muco-adhesive polymer which binds to cornea. Within furtherembodiments, the anti-angiogenic factors or anti-angiogenic compositionsmay be utilized as an adjunct to conventional steroid therapy. Topicaltherapy may also be useful prophylactically in corneal lesions which areknown to have a high probability of inducing an angiogenic response(such as chemical burns). In these instances the treatment, likely incombination with steroids, may be instituted immediately to help preventsubsequent complications.

Within other embodiments, the compounds described above may be injecteddirectly into the corneal stroma by an ophthalmologist under microscopicguidance. The preferred site of injection may vary with the morphologyof the individual lesion, but the goal of the administration would be toplace the composition at the advancing front of the vasculature (i.e.,interspersed between the blood vessels and the normal cornea). In mostcases this would involve perilimbic corneal injection to “protect” thecornea from the advancing blood vessels. This method may also beutilized shortly after a corneal insult in order to prophylacticallyprevent corneal neovascularization. In this situation the material couldbe injected in the perilimbic cornea interspersed between the corneallesion and its undesired potential limbic blood supply. Such methods mayalso be utilized in a similar fashion to prevent capillary invasion oftransplanted corneas. In a sustained-release form injections might onlybe required 2-3 times per year. A steroid could also be added to theinjection solution to reduce inflammation resulting from the injectionitself.

Within another aspect of the present invention, methods are provided fortreating neovascular glaucoma, comprising the step of administering to apatient a therapeutically effective amount of an albumin fusion proteinof the invention and/or polynucleotides encoding an albumin fusionprotein of the invention to the eye, such that the formation of bloodvessels is inhibited. In one embodiment, the compound may beadministered topically to the eye in order to treat early forms ofneovascular glaucoma. Within other embodiments, the compound may beimplanted by injection into the region of the anterior chamber angle.Within other embodiments, the compound may also be placed in anylocation such that the compound is continuously released into theaqueous humor. Within another aspect of the present invention, methodsare provided for treating proliferative diabetic retinopathy, comprisingthe step of administering to a patient a therapeutically effectiveamount of an albumin fusion protein of the invention and/orpolynucleotides encoding an albumin fusion protein of the invention tothe eyes, such that the formation of blood vessels is inhibited.

Within particularly preferred embodiments of the invention,proliferative diabetic retinopathy may be treated by injection into theaqueous humor or the vitreous, in order to increase the localconcentration of the polynucleotide, polypeptide, antagonist and/oragonist in the retina. Preferably, this treatment should be initiatedprior to the acquisition of severe disease requiring photocoagulation.

Within another aspect of the present invention, methods are provided fortreating retrolental fibroplasia, comprising the step of administeringto a patient a therapeutically effective amount of an albumin fusionprotein of the invention and/or polynucleotides encoding an albuminfusion protein of the invention to the eye, such that the formation ofblood vessels is inhibited. The compound may be administered topically,via intravitreous injection and/or via intraocular implants.

Additionally, disorders which can be treated with fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention include, but are not limited to, hemangioma, arthritis,psoriasis, angiofibroma, atherosclerotic plaques, delayed wound healing,granulations, hemophilic joints, hypertrophic scars, nonunion fractures,Osler-Weber syndrome, pyogenic granuloma, scleroderma, trachoma, andvascular adhesions.

Moreover, disorders and/or states, which can be treated, prevented,diagnosed, and/or prognosed with the albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention of the invention include, but are not limited to, solidtumors, blood born tumors such as leukemias, tumor metastasis, Kaposi'ssarcoma, benign tumors, for example hemangiomas, acoustic neuromas,neurofibromas, trachomas, and pyogenic granulomas, rheumatoid arthritis,psoriasis, ocular angiogenic diseases, for example, diabeticretinopathy, retinopathy of prematurity, macular degeneration, cornealgraft rejection, neovascular glaucoma, retrolental fibroplasia,rubeosis, retinoblastoma, and uvietis, delayed wound healing,endometriosis, vascluogenesis, granulations, hypertrophic scars(keloids), nonunion fractures, scleroderma, trachoma, vascularadhesions, myocardial angiogenesis, coronary collaterals, cerebralcollaterals, arteriovenous malformations, ischemic limb angiogenesis,Osler-Webber Syndrome, plaque neovascularization, telangiectasia,hemophiliac joints, angiofibroma fibromuscular dysplasia, woundgranulation, Crohn's disease, atherosclerosis, birth control agent bypreventing vascularization required for embryo implantation controllingmenstruation, diseases that have angiogenesis as a pathologicconsequence such as cat scratch disease (Rochele minalia quintosa),ulcers (Helicobacter pylori), Bartonellosis and bacillary angiomatosis.

In one aspect of the birth control method, an amount of the compoundsufficient to block embryo implantation is administered before or afterintercourse and fertilization have occurred, thus providing an effectivemethod of birth control, possibly a “morning after” method. Albuminfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention may also be used in controllingmenstruation or administered as either a peritoneal lavage fluid or forperitoneal implantation in the treatment of endometriosis.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be incorporated intosurgical sutures in order to prevent stitch granulomas.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may be utilized in a widevariety of surgical procedures. For example, within one aspect of thepresent invention a compositions (in the form of, for example, a sprayor film) may be utilized to coat or spray an area prior to removal of atumor, in order to isolate normal surrounding tissues from malignanttissue, and/or to prevent the spread of disease to surrounding tissues.Within other aspects of the present invention, compositions (e.g., inthe form of a spray) may be delivered via endoscopic procedures in orderto coat tumors, or inhibit angiogenesis in a desired locale. Within yetother aspects of the present invention, surgical meshes which have beencoated with anti-angiogenic compositions of the present invention may beutilized in any procedure wherein a surgical mesh might be utilized. Forexample, within one embodiment of the invention a surgical mesh ladenwith an anti-angiogenic composition may be utilized during abdominalcancer resection surgery (e.g., subsequent to colon resection) in orderto provide support to the structure, and to release an amount of theanti-angiogenic factor.

Within further aspects of the present invention, methods are providedfor treating tumor excision sites, comprising administering albuminfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention to the resection margins of a tumorsubsequent to excision, such that the local recurrence of cancer and theformation of new blood vessels at the site is inhibited. Within oneembodiment of the invention, the anti-angiogenic compound isadministered directly to the tumor excision site (e.g., applied byswabbing, brushing or otherwise coating the resection margins of thetumor with the anti-angiogenic compound). Alternatively, theanti-angiogenic compounds may be incorporated into known surgical pastesprior to administration. Within particularly preferred embodiments ofthe invention, the anti-angiogenic compounds are applied after hepaticresections for malignancy, and after neurosurgical operations.

Within one aspect of the present invention, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may be administered to the resection margin of a wide varietyof tumors, including for example, breast, colon, brain and hepatictumors. For example, within one embodiment of the invention,anti-angiogenic compounds may be administered to the site of aneurological tumor subsequent to excision, such that the formation ofnew blood vessels at the site are inhibited.

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may also beadministered along with other anti-angiogenic factors. Representativeexamples of other anti-angiogenic factors include: Anti-Invasive Factor,retinoic acid and derivatives thereof, paclitaxel, Suramin, TissueInhibitor of Metalloproteinase-1, Tissue Inhibitor ofMetalloproteinase-2, Plasminogen Activator Inhibitor-1, PlasminogenActivator Inhibitor-2, and various forms of the lighter “d group”transition metals.

Lighter “d group” transition metals include, for example, vanadium,molybdenum, tungsten, titanium, niobium, and tantalum species. Suchtransition metal species may form transition metal complexes. Suitablecomplexes of the above-mentioned transition metal species include oxotransition metal complexes.

Representative examples of vanadium complexes include oxo vanadiumcomplexes such as vanadate and vanadyl complexes. Suitable vanadatecomplexes include metavanadate and orthovanadate complexes such as, forexample, ammonium metavanadate, sodium metavanadate, and sodiumorthovanadate. Suitable vanadyl complexes include, for example, vanadylacetylacetonate and vanadyl sulfate including vanadyl sulfate hydratessuch as vanadyl sulfate mono- and trihydrates.

Representative examples of tungsten and molybdenum complexes alsoinclude oxo complexes. Suitable oxo tungsten complexes include tungstateand tungsten oxide complexes. Suitable tungstate complexes includeammonium tungstate, calcium tungstate, sodium tungstate dihydrate, andtungstic acid. Suitable tungsten oxides include tungsten (IV) oxide andtungsten (VI) oxide. Suitable oxo molybdenum complexes includemolybdate, molybdenum oxide, and molybdenyl complexes. Suitablemolybdate complexes include ammonium molybdate and its hydrates, sodiummolybdate and its hydrates, and potassium molybdate and its hydrates.Suitable molybdenum oxides include molybdenum (VI) oxide, molybdenum(VI) oxide, and molybdic acid. Suitable molybdenyl complexes include,for example, molybdenyl acetylacetonate. Other suitable tungsten andmolybdenum complexes include hydroxo derivatives derived from, forexample, glycerol, tartaric acid, and sugars.

A wide variety of other anti-angiogenic factors may also be utilizedwithin the context of the present invention. Representative examplesinclude platelet factor 4; protamine sulphate; sulphated chitinderivatives (prepared from queen crab shells), (Murata et al., CancerRes. 51:22-26, 1991); Sulphated Polysaccharide Peptidoglycan Complex(SP-PG) (the function of this compound may be enhanced by the presenceof steroids such as estrogen, and tamoxifen citrate); Staurosporine;modulators of matrix metabolism, including for example, proline analogs,cishydroxyproline, d,L-3,4-dehydroproline, Thiaproline,alpha,alpha-dipyridyl, aminopropionitrile fumarate;4-propyl-5-(4-pyridinyl)-2(3H)-oxazolone; Methotrexate; Mitoxantrone;Heparin; Interferons; 2 Macroglobulin-serum; ChIMP-3 (Pavloff et al., J.Bio. Chem. 267:17321-17326, (1992)); Chymostatin (Tomkinson et al.,Biochem J. 286:475-480, (1992)); Cyclodextrin Tetradecasulfate;Eponemycin; Camptothecin; Fumagillin (Ingber et al., Nature 348:555-557,1990); Gold Sodium Thiomalate (“GST”; Matsubara and Ziff, J. Clin.Invest. 79:1440-1446, (1987)); anticollagenase-serum; alpha2-antiplasmin(Holmes et al., J. Biol. Chem. 262(4):1659-1664, (1987)); Bisantrene(National Cancer Institute); Lobenzarit disodium(N-(2)-carboxyphenyl-4-chloroanthronilic acid disodium or “CCA”;Takeuchi et al., Agents Actions 36:312-316, (1992)); Thalidomide;Angiostatic steroid; AGM-1470; carboxynaminolmidazole; andmetalloproteinase inhibitors such as BB94.

Diseases at the Cellular Level

Diseases associated with increased cell survival or the inhibition ofapoptosis that could be treated, prevented, diagnosed, and/or prognosedusing fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, include cancers (such asfollicular lymphomas, carcinomas with p53 mutations, andhormone-dependent tumors, including, but not limited to colon cancer,cardiac tumors, pancreatic cancer, melanoma, retinoblastoma,glioblastoma, lung cancer, intestinal cancer, testicular cancer, stomachcancer, neuroblastoma, myxoma, myoma, lymphoma, endothelioma,osteoblastoma, osteoclastoma, osteosarcoma, chondrosarcoma, adenoma,breast cancer, prostate cancer, Kaposi's sarcoma and ovarian cancer);autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome,Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn'sdisease, polymyositis, systemic lupus erythematosus and immune-relatedglomerulonephritis and rheumatoid arthritis) and viral infections (suchas herpes viruses, pox viruses and adenoviruses), inflammation, graft v.host disease, acute graft rejection, and chronic graft rejection.

In preferred embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to inhibit growth, progression, and/or metasis of cancers, inparticular those listed above.

Additional diseases or conditions associated with increased cellsurvival that could be treated or detected by fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention include, but are not limited to, progression, and/ormetastases of malignancies and related disorders such as leukemia(including acute leukemias (e.g., acute lymphocytic leukemia, acutemyelocytic leukemia (including myeloblastic, promyelocytic,myelomonocytic, monocytic, and erythroleukemia)) and chronic leukemias(e.g., chronic myelocytic (granulocytic) leukemia and chroniclymphocytic leukemia)), polycythemia vera, lymphomas (e.g., Hodgkin'sdisease and non-Hodgkin's disease), multiple myeloma, Waldenstrom'smacroglobulinemia, heavy chain disease, and solid tumors including, butnot limited to, sarcomas and carcinomas such as fibrosarcoma,myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma,angiosarcoma, endotheliosarcoma, lymphangiosarcoma,lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor,leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer,breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma,basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceousgland carcinoma, papillary carcinoma, papillary adenocarcinomas,cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renalcell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma,seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testiculartumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma,epithelial carcinoma, glioma, astrocytoma, medulloblastoma,craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acousticneuroma, oligodendroglioma, menangioma, melanoma, neuroblastoma, andretinoblastoma.

Diseases associated with increased apoptosis that could be treated,prevented, diagnosed, and/or prognesed using fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention, include, but are not limited to, AIDS; neurodegenerativedisorders (such as Alzheimer's disease, Parkinson's disease, Amyotrophiclateral sclerosis, Retinitis pigmentosa, Cerebellar degeneration andbrain tumor or prior associated disease); autoimmune disorders (such as,multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliarycirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemiclupus erythematosus and immune-related glomerulonephritis and rheumatoidarthritis) myelodysplastic syndromes (such as aplastic anemia), graft v.host disease, ischemic injury (such as that caused by myocardialinfarction, stroke and reperfusion injury), liver injury (e.g.,hepatitis related liver injury, ischemia/reperfusion injury, cholestosis(bile duct injury) and liver cancer); toxin-induced liver disease (suchas that caused by alcohol), septic shock, cachexia and anorexia.

Wound Healing and Epithelial Cell Proliferation

In accordance with yet a further aspect of the present invention, thereis provided a process for utilizing fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention, for therapeutic purposes, for example, to stimulateepithelial cell proliferation and basal keratinocytes for the purpose ofwound healing, and to stimulate hair follicle production and healing ofdermal wounds. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, maybe clinically useful in stimulating wound healing including surgicalwounds, excisional wounds, deep wounds involving damage of the dermisand epidermis, eye tissue wounds, dental tissue wounds, oral cavitywounds, diabetic ulcers, dermal ulcers, cubitus ulcers, arterial ulcers,venous stasis ulcers, burns resulting from heat exposure or chemicals,and other abnormal wound healing conditions such as uremia,malnutrition, vitamin deficiencies and complications associated withsystemic treatment with steroids, radiation therapy and antineoplasticdrugs and antimetabolites. Albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention, could be used to promote dermal reestablishment subsequent todermal loss

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could be used to increase theadherence of skin grafts to a wound bed and to stimulatere-epithelialization from the wound bed. The following are types ofgrafts that fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, could be used toincrease adherence to a wound bed: autografts, artificial skin,allografts, autodermic graft, autoepdermic grafts, avacular grafts,Blair-Brown grafts, bone graft, brephoplastic grafts, cutis graft,delayed graft, dermic graft, epidermic graft, fascia graft, fullthickness graft, heterologous graft, xenograft, homologous graft,hyperplastic graft, lamellar graft, mesh graft, mucosal graft,Ollier-Thiersch graft, omenpal graft, patch graft, pedicle graft,penetrating graft, split skin graft, thick split graft. Albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention, can be used to promote skin strength and toimprove the appearance of aged skin.

It is believed that fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, willalso produce changes in hepatocyte proliferation, and epithelial cellproliferation in the lung, breast, pancreas, stomach, small intestine,and large intestine. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, couldpromote proliferation of epithelial cells such as sebocytes, hairfollicles, hepatocytes, type II pneumocytes, mucin-producing gobletcells, and other epithelial cells and their progenitors contained withinthe skin, lung, liver, and gastrointestinal tract. Albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention, may promote proliferation of endothelialcells, keratinocytes, and basal keratinocytes.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could also be used to reducethe side effects of gut toxicity that result from radiation,chemotherapy treatments or viral infections. Albumin fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention, may have a cytoprotective effect on the small intestinemucosa. Albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, may also stimulatehealing of mucositis (mouth ulcers) that result from chemotherapy andviral infections.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could further be used in fullregeneration of skin in full and partial thickness skin defects,including burns, (i.e., repopulation of hair follicles, sweat glands,and sebaceous glands), treatment of other skin defects such aspsoriasis. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, couldbe used to treat epidermolysis bullosa, a defect in adherence of theepidermis to the underlying dermis which results in frequent, open andpainful blisters by accelerating reepithelialization of these lesions.Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could also be used to treatgastric and doudenal ulcers and help heal by scar formation of themucosal lining and regeneration of glandular mucosa and duodenal mucosallining more rapidly. Inflammatory bowel diseases, such as Crohn'sdisease and ulcerative colitis, are diseases which result in destructionof the mucosal surface of the small or large intestine, respectively.Thus, fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could be used to promote theresurfacing of the mucosal surface to aid more rapid healing and toprevent progression of inflammatory bowel disease. Treatment with fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention, is expected to have a significant effect onthe production of mucus throughout the gastrointestinal tract and couldbe used to protect the intestinal mucosa from injurious substances thatare ingested or following surgery. Albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention, could be used to treat diseases associate with the underexpression.

Moreover, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, could be used toprevent and heal damage to the lungs due to various pathological states.Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, which could stimulateproliferation and differentiation and promote the repair of alveoli andbronchiolar epithelium to prevent or treat acute or chronic lung damage.For example, emphysema, which results in the progressive loss of aveoli,and inhalation injuries, i.e., resulting from smoke inhalation andburns, that cause necrosis of the bronchiolar epithelium and alveolicould be effectively treated using polynucleotides or polypeptides,agonists or antagonists of the present invention. Also fusion proteinsof the invention and/or polynucleotides encoding albumin fusion proteinsof the invention, could be used to stimulate the proliferation of anddifferentiation of type II pneumocytes, which may help treat or preventdisease such as hyaline membrane diseases, such as infant respiratorydistress syndrome and bronchopulmonary displasia, in premature infants.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, could stimulate theproliferation and differentiation of hepatocytes and, thus, could beused to alleviate or treat liver diseases and pathologies such asfulminant liver failure caused by cirrhosis, liver damage caused byviral hepatitis and toxic substances (i.e., acetaminophen, carbontetrachloride and other hepatotoxins known in the art).

In addition, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, could be used treator prevent the onset of diabetes mellitus. In patients with newlydiagnosed Types I and II diabetes, where some islet cell functionremains, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, could be used tomaintain the islet function so as to alleviate, delay or preventpermanent manifestation of the disease. Also, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention, could be used as an auxiliary in islet cell transplantationto improve or promote islet cell function.

Neural Activity and Neurological Diseases

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be used for thediagnosis and/or treatment of diseases, disorders, damage or injury ofthe brain and/or nervous system. Nervous system disorders that can betreated with the compositions of the invention (e.g., fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention), include, but are not limited to, nervous systeminjuries, and diseases or disorders which result in either adisconnection of axons, a diminution or degeneration of neurons, ordemyelination. Nervous system lesions which may be treated in a patient(including human and non-human mammalian patients) according to themethods of the invention, include but are not limited to, the followinglesions of either the central (including spinal cord, brain) orperipheral nervous systems: (1) ischemic lesions, in which a lack ofoxygen in a portion of the nervous system results in neuronal injury ordeath, including cerebral infarction or ischemia, or spinal cordinfarction or ischemia; (2) traumatic lesions, including lesions causedby physical injury or associated with surgery, for example, lesionswhich sever a portion of the nervous system, or compression injuries;(3) malignant lesions, in which a portion of the nervous system isdestroyed or injured by malignant tissue which is either a nervoussystem associated malignancy or a malignancy derived from non-nervoussystem tissue; (4) infectious lesions, in which a portion of the nervoussystem is destroyed or injured as a result of infection, for example, byan abscess or associated with infection by human immunodeficiency virus,herpes zoster, or herpes simplex virus or with Lyme disease,tuberculosis, or syphilis; (5) degenerative lesions, in which a portionof the nervous system is destroyed or injured as a result of adegenerative process including but not limited to, degenerationassociated with Parkinson's disease, Alzheimer's disease, Huntington'schorea, or amyotrophic lateral sclerosis (ALS); (6) lesions associatedwith nutritional diseases or disorders, in which a portion of thenervous system is destroyed or injured by a nutritional disorder ordisorder of metabolism including, but not limited to, vitamin B12deficiency, folic acid deficiency, Wernicke disease, tobacco-alcoholamblyopia, Marchiafava-Bignami disease (primary degeneration of thecorpus callosum), and alcoholic cerebellar degeneration; (7)neurological lesions associated with systemic diseases including, butnot limited to, diabetes (diabetic neuropathy, Bell's palsy), systemiclupus erythematosus, carcinoma, or sarcoidosis; (8) lesions caused bytoxic substances including alcohol, lead, or particular neurotoxins; and(9) demyelinated lesions in which a portion of the nervous system isdestroyed or injured by a demyelinating disease including, but notlimited to, multiple sclerosis, human immunodeficiency virus-associatedmyelopathy, transverse myelopathy or various etiologies, progressivemultifocal leukoencephalopathy, and central pontine myelinolysis.

In one embodiment, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to protect neural cells from the damaging effects of hypoxia. In afurther preferred embodiment, the albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used to protect neural cells from the damaging effects ofcerebral hypoxia. According to this embodiment, the compositions of theinvention are used to treat or prevent neural cell injury associatedwith cerebral hypoxia. In one non-exclusive aspect of this embodiment,the albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, are used to treat orprevent neural cell injury associated with cerebral ischemia. In anothernon-exclusive aspect of this embodiment, the albumin fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention are used to treat or prevent neural cell injury associatedwith cerebral infarction.

In another preferred embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used to treat or prevent neural cell injury associatedwith a stroke. In a specific embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used to treat or prevent cerebral neural cell injuryassociated with a stroke.

In another preferred embodiment, albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention are used to treat or prevent neural cell injury associatedwith a heart attack. In a specific embodiment, albumin fusion proteinsof the invention and/or polynucleotides encoding albumin fusion proteinsof the invention are used to treat or prevent cerebral neural cellinjury associated with a heart attack.

The compositions of the invention which are useful for treating orpreventing a nervous system disorder may be selected by testing forbiological activity in promoting the survival or differentiation ofneurons. For example, and not by way of limitation, compositions of theinvention which elicit any of the following effects may be usefulaccording to the invention: (1) increased survival time of neurons inculture either in the presence or absence of hypoxia or hypoxicconditions; (2) increased sprouting of neurons in culture or in vivo;(3) increased production of a neuron-associated molecule in culture orin vivo, e.g., choline acetyltransferase or acetylcholinesterase withrespect to motor neurons; or (4) decreased symptoms of neurondysfunction in vivo. Such effects may be measured by any method known inthe art. In preferred, non-limiting embodiments, increased survival ofneurons may routinely be measured using a method set forth herein orotherwise known in the art, such as, for example, in Zhang et al., ProcNatl Acad Sci USA 97:3637-42 (2000) or in Arakawa et al., J. Neurosci.,10:3507-15 (1990); increased sprouting of neurons may be detected bymethods known in the art, such as, for example, the methods set forth inPestronk et al., Exp. Neurol., 70:65-82 (1980), or Brown et al., Ann.Rev. Neurosci., 4:17-42 (1981); increased production ofneuron-associated molecules may be measured by bioassay, enzymaticassay, antibody binding, Northern blot assay, etc., using techniquesknown in the art and depending on the molecule to be measured; and motorneuron dysfunction may be measured by assessing the physicalmanifestation of motor neuron disorder, e.g., weakness, motor neuronconduction velocity, or functional disability.

In specific embodiments, motor neuron disorders that may be treatedaccording to the invention include, but are not limited to, disorderssuch as infarction, infection, exposure to toxin, trauma, surgicaldamage, degenerative disease or malignancy that may affect motor neuronsas well as other components of the nervous system, as well as disordersthat selectively affect neurons such as amyotrophic lateral sclerosis,and including, but not limited to, progressive spinal muscular atrophy,progressive bulbar palsy, primary lateral sclerosis, infantile andjuvenile muscular atrophy, progressive bulbar paralysis of childhood(Fazio-Londe syndrome), poliomyelitis and the post polio syndrome, andHereditary Motorsensory Neuropathy (Charcot-Marie-Tooth Disease).

Further, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may play a role inneuronal survival; synapse formation; conductance; neuraldifferentiation, etc. Thus, compositions of the invention (includingfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention) may be used to diagnose and/or treator prevent diseases or disorders associated with these roles, including,but not limited to, learning and/or cognition disorders. Thecompositions of the invention may also be useful in the treatment orprevention of neurodegenerative disease states and/or behaviouraldisorders. Such neurodegenerative disease states and/or behavioraldisorders include, but are not limited to, Alzheimer's Disease,Parkinson's Disease, Huntington's Disease, Tourette Syndrome,schizophrenia, mania, dementia, paranoia, obsessive compulsive disorder,panic disorder, learning disabilities, ALS, psychoses, autism, andaltered behaviors, including disorders in feeding, sleep patterns,balance, and perception. In addition, compositions of the invention mayalso play a role in the treatment, prevention and/or detection ofdevelopmental disorders associated with the developing embryo, orsexually-linked disorders.

Additionally, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, may be useful inprotecting neural cells from diseases, damage, disorders, or injury,associated with cerebrovascular disorders including, but not limited to,carotid artery diseases (e.g., carotid artery thrombosis, carotidstenosis, or Moyamoya Disease), cerebral amyloid angiopathy, cerebralaneurysm, cerebral anoxia, cerebral arteriosclerosis, cerebralarteriovenous malformations, cerebral artery diseases, cerebral embolismand thrombosis (e.g., carotid artery thrombosis, sinus thrombosis, orWallenberg's Syndrome), cerebral hemorrhage (e.g., epidural or subduralhematoma, or subarachnoid hemorrhage), cerebral infarction, cerebralischemia (e.g., transient cerebral ischemia, Subclavian Steal Syndrome,or vertebrobasilar insufficiency), vascular dementia (e.g.,multi-infarct), leukomalacia, periventricular, and vascular headache(e.g., cluster headache or migraines).

In accordance with yet a further aspect of the present invention, thereis provided a process for utilizing fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of theinvention, for therapeutic purposes, for example, to stimulateneurological cell proliferation and/or differentiation. Therefore,fusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention may be used to treat and/or detectneurologic diseases. Moreover, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, canbe used as a marker or detector of a particular nervous system diseaseor disorder.

Examples of neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include, brain diseases, such asmetabolic brain diseases which includes phenylketonuria such as maternalphenylketonuria, pyruvate carboxylase deficiency, pyruvate dehydrogenasecomplex deficiency, Wernicke's Encephalopathy, brain edema, brainneoplasms such as cerebellar neoplasms which include infratentorialneoplasms, cerebral ventricle neoplasms such as choroid plexusneoplasms, hypothalamic neoplasms, supratentorial neoplasms, canavandisease, cerebellar diseases such as cerebellar ataxia which includespinocerebellar degeneration such as ataxia telangiectasia, cerebellardyssynergia, Friederich's Ataxia, Machado-Joseph Disease,olivopontocerebellar atrophy, cerebellar neoplasms such asinfratentorial neoplasms, diffuse cerebral sclerosis such asencephalitis periaxialis, globoid cell leukodystrophy, metachromaticleukodystrophy and subacute sclerosing panencephalitis.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include cerebrovascular disorders (suchas carotid artery diseases which include carotid artery thrombosis,carotid stenosis and Moyamoya Disease), cerebral amyloid angiopathy,cerebral aneurysm, cerebral anoxia, cerebral arteriosclerosis, cerebralarteriovenous malformations, cerebral artery diseases, cerebral embolismand thrombosis such as carotid artery thrombosis, sinus thrombosis andWallenberg's Syndrome, cerebral hemorrhage such as epidural hematoma,subdural hematoma and subarachnoid hemorrhage, cerebral infarction,cerebral ischemia such as transient cerebral ischemia, Subclavian StealSyndrome and vertebrobasilar insufficiency, vascular dementia such asmulti-infarct dementia, periventricular leukomalacia, vascular headachesuch as cluster headache and migraine.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include dementia such as AIDS DementiaComplex, presenile dementia such as Alzheimer's Disease andCreutzfeldt-Jakob Syndrome, senile dementia such as Alzheimer's Diseaseand progressive supranuclear palsy, vascular dementia such asmulti-infarct dementia, encephalitis which include encephalitisperiaxialis, viral encephalitis such as epidemic encephalitis, JapaneseEncephalitis, St. Louis Encephalitis, tick-borne encephalitis and WestNile Fever, acute disseminated encephalomyelitis, meningoencephalitissuch as uveomeningoencephalitic syndrome, Postencephalitic ParkinsonDisease and subacute sclerosing panencephalitis, encephalomalacia suchas periventricular leukomalacia, epilepsy such as generalized epilepsywhich includes infantile spasms, absence epilepsy, myoclonic epilepsywhich includes MERRF Syndrome, tonic-clonic epilepsy, partial epilepsysuch as complex partial epilepsy, frontal lobe epilepsy and temporallobe epilepsy, post-traumatic epilepsy, status epilepticus such asEpilepsia Partialis Continua, and Hallervorden-Spatz Syndrome.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include hydrocephalus such asDandy-Walker Syndrome and normal pressure hydrocephalus, hypothalamicdiseases such as hypothalamic neoplasms, cerebral malaria, narcolepsywhich includes cataplexy, bulbar poliomyelitis, cerebri pseudotumor,Rett Syndrome, Reye's Syndrome, thalamic diseases, cerebraltoxoplasmosis, intracranial tuberculoma and Zellweger Syndrome, centralnervous system infections such as AIDS Dementia Complex, Brain Abscess,subdural empyema, encephalomyelitis such as Equine Encephalomyelitis,Venezuelan Equine Encephalomyelitis, Necrotizing HemorrhagicEncephalomyelitis, Visna, and cerebral malaria.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include meningitis such asarachnoiditis, aseptic meningtitis such as viral meningtitis whichincludes lymphocytic choriomeningitis, Bacterial meningtitis whichincludes Haemophilus Meningtitis, Listeria Meningtitis, MeningococcalMeningtitis such as Waterhouse-Friderichsen Syndrome, PneumococcalMeningtitis and meningeal tuberculosis, fungal meningitis such asCryptococcal Meningtitis, subdural effusion, meningoencephalitis such asuvemeningoencephalitic syndrome, myelitis such as transverse myelitis,neurosyphilis such as tabes dorsalis, poliomyelitis which includesbulbar poliomyelitis and postpoliomyelitis syndrome, prion diseases(such as Creutzfeldt-Jakob Syndrome, Bovine Spongiform Encephalopathy,Gerstmann-Straussler Syndrome, Kuru, Scrapie), and cerebraltoxoplasmosis.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include central nervous systemneoplasms such as brain neoplasms that include cerebellar neoplasms suchas infratentorial neoplasms, cerebral ventricle neoplasms such aschoroid plexus neoplasms, hypothalamic neoplasms and supratentorialneoplasms, meningeal neoplasms, spinal cord neoplasms which includeepidural neoplasms, demyelinating diseases such as Canavan Diseases,diffuse cerebral sceloris which includes adrenoleukodystrophy,encephalitis periaxialis, globoid cell leukodystrophy, diffuse cerebralsclerosis such as metachromatic leukodystrophy, allergicencephalomyelitis, necrotizing hemorrhagic encephalomyelitis,progressive multifocal leukoencephalopathy, multiple sclerosis, centralpontine myelinolysis, transverse myelitis, neuromyelitis optica,Scrapie, Swayback, Chronic Fatigue Syndrome, Visna, High PressureNervous Syndrome, Meningism, spinal cord diseases such as amyotoniacongenita, amyotrophic lateral sclerosis, spinal muscular atrophy suchas Werdnig-Hoffmann Disease, spinal cord compression, spinal cordneoplasms such as epidural neoplasms, syringomyelia, Tabes Dorsalis,Stiff-Man Syndrome, mental retardation such as Angelman Syndrome,Cri-du-Chat Syndrome, De Lange's Syndrome, Down Syndrome, Gangliosidosessuch as gangliosidoses G(M1), Sandhoff Disease, Tay-Sachs Disease,Hartnup Disease, homocystinuria, Laurence-Moon-Biedl Syndrome,Lesch-Nyhan Syndrome, Maple Syrup Urine Disease, mucolipidosis such asfucosidosis, neuronal ceroid-lipofuscinosis, oculocerebrorenal syndrome,phenylketonuria such as maternal phenylketonuria, Prader-Willi Syndrome,Rett Syndrome, Rubinstein-Taybi Syndrome, Tuberous Sclerosis, WAGRSyndrome, nervous system abnormalities such as holoprosencephaly, neuraltube defects such as anencephaly which includes hydrangencephaly,Arnold-Chairi Deformity, encephalocele, meningocele, meningomyelocele,spinal dysraphism such as spina bifida cystica and spina bifida occulta.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include hereditary motor and sensoryneuropathies which include Charcot-Marie Disease, Hereditary opticatrophy, Refsum's Disease, hereditary spastic paraplegia,Werdnig-Hoffmann Disease, Hereditary Sensory and Autonomic Neuropathiessuch as Congenital Analgesia and Familial Dysautonomia, Neurologicmanifestations (such as agnosia that include Gerstmann's Syndrome,Amnesia such as retrograde amnesia, apraxia, neurogenic bladder,cataplexy, communicative disorders such as hearing disorders thatincludes deafness, partial hearing loss, loudness recruitment andtinnitus, language disorders such as aphasia which include agraphia,anomia, broca aphasia, and Wernicke Aphasia, Dyslexia such as AcquiredDyslexia, language development disorders, speech disorders such asaphasia which includes anomia, broca aphasia and Wernicke Aphasia,articulation disorders, communicative disorders such as speech disorderswhich include dysarthria, echolalia, mutism and stuttering, voicedisorders such as aphonia and hoarseness, decerebrate state, delirium,fasciculation, hallucinations, meningism, movement disorders such asangelman syndrome, ataxia, athetosis, chorea, dystonia, hypokinesia,muscle hypotonia, myoclonus, tic, torticollis and tremor, musclehypertonia such as muscle rigidity such as stiff-man syndrome, musclespasticity, paralysis such as facial paralysis which includes HerpesZoster Oticus, Gastroparesis, Hemiplegia, ophthalmoplegia such asdiplopia, Duane's Syndrome, Homer's Syndrome, Chronic progressiveexternal ophthalmoplegia such as Kearns Syndrome, Bulbar Paralysis,Tropical Spastic Paraparesis, Paraplegia such as Brown-Sequard Syndrome,quadriplegia, respiratory paralysis and vocal cord paralysis, paresis,phantom limb, taste disorders such as ageusia and dysgeusia, visiondisorders such as amblyopia, blindness, color vision defects, diplopia,hemianopsia, scotoma and subnormal vision, sleep disorders such ashypersomnia which includes Kleine-Levin Syndrome, insomnia, andsomnambulism, spasm such as trismus, unconsciousness such as coma,persistent vegetative state and syncope and vertigo, neuromusculardiseases such as amyotonia congenita, amyotrophic lateral sclerosis,Lambert-Eaton Myasthenic Syndrome, motor neuron disease, muscularatrophy such as spinal muscular atrophy, Charcot-Marie Disease andWerdnig-Hoffmann Disease, Postpoliomyelitis Syndrome, MuscularDystrophy, Myasthenia Gravis, Myotonia Atrophica, Myotonia Confenita,Nemaline Myopathy, Familial Periodic Paralysis, MultiplexParamyloclonus, Tropical Spastic Paraparesis and Stiff-Man Syndrome,peripheral nervous system diseases such as acrodynia, amyloidneuropathies, autonomic nervous system diseases such as Adie's Syndrome,Barre-Lieou Syndrome, Familial Dysautonomia, Homer's Syndrome, ReflexSympathetic Dystrophy and Shy-Drager Syndrome, Cranial Nerve Diseasessuch as Acoustic Nerve Diseases such as Acoustic Neuroma which includesNeurofibromatosis 2, Facial Nerve Diseases such as Facial Neuralgia,Melkersson-Rosenthal Syndrome, ocular motility disorders which includesamblyopia, nystagmus, oculomotor nerve paralysis, ophthalmoplegia suchas Duane's Syndrome, Horner's Syndrome, Chronic Progressive ExternalOphthalmoplegia which includes Kearns Syndrome, Strabismus such asEsotropia and Exotropia, Oculomotor Nerve Paralysis, Optic NerveDiseases such as Optic Atrophy which includes Hereditary Optic Atrophy,Optic Disk Drusen, Optic Neuritis such as Neuromyelitis Optica,Papilledema, Trigeminal Neuralgia, Vocal Cord Paralysis, DemyelinatingDiseases such as Neuromyelitis Optica and Swayback, and Diabeticneuropathies such as diabetic foot.

Additional neurologic diseases which can be treated or detected withfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention include nerve compression syndromessuch as carpal tunnel syndrome, tarsal tunnel syndrome, thoracic outletsyndrome such as cervical rib syndrome, ulnar nerve compressionsyndrome, neuralgia such as causalgia, cervico-brachial neuralgia,facial neuralgia and trigeminal neuralgia, neuritis such as experimentalallergic neuritis, optic neuritis, polyneuritis, polyradiculoneuritisand radiculities such as polyradiculitis, hereditary motor and sensoryneuropathies such as Charcot-Marie Disease, Hereditary Optic Atrophy,Refsum's Disease, Hereditary Spastic Paraplegia and Werdnig-HoffmannDisease, Hereditary Sensory and Autonomic Neuropathies which includeCongenital Analgesia and Familial Dysautonomia, POEMS Syndrome,Sciatica, Gustatory Sweating and Tetany).

Endocrine Disorders

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, may be used to treat, prevent,diagnose, and/or prognose disorders and/or diseases related to hormoneimbalance, and/or disorders or diseases of the endocrine system.

Hormones secreted by the glands of the endocrine system control physicalgrowth, sexual function, metabolism, and other functions. Disorders maybe classified in two ways: disturbances in the production of hormones,and the inability of tissues to respond to hormones. The etiology ofthese hormone imbalance or endocrine system diseases, disorders orconditions may be genetic, somatic, such as cancer and some autoimmunediseases, acquired (e.g., by chemotherapy, injury or toxins), orinfectious. Moreover, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention can beused as a marker or detector of a particular disease or disorder relatedto the endocrine system and/or hormone imbalance.

Endocrine system and/or hormone imbalance and/or diseases encompassdisorders of uterine motility including, but not limited to:complications with pregnancy and labor (e.g., pre-term labor, post-termpregnancy, spontaneous abortion, and slow or stopped labor); anddisorders and/or diseases of the menstrual cycle (e.g., dysmenorrhea andendometriosis).

Endocrine system and/or hormone imbalance disorders and/or diseasesinclude disorders and/or diseases of the pancreas, such as, for example,diabetes mellitus, diabetes insipidus, congenital pancreatic agenesis,pheochromocytoma-islet cell tumor syndrome; disorders and/or diseases ofthe adrenal glands such as, for example, Addison's Disease,corticosteroid deficiency, virilizing disease, hirsutism, Cushing'sSyndrome, hyperaldosteronism, pheochromocytoma; disorders and/ordiseases of the pituitary gland, such as, for example, hyperpituitarism,hypopituitarism, pituitary dwarfism, pituitary adenoma,panhypopituitarism, acromegaly, gigantism; disorders and/or diseases ofthe thyroid, including but not limited to, hyperthyroidism,hypothyroidism, Plummer's disease, Graves' disease (toxic diffusegoiter), toxic nodular goiter, thyroiditis (Hashimoto's thyroiditis,subacute granulomatous thyroiditis, and silent lymphocytic thyroiditis),Pendred's syndrome, myxedema, cretinism, thyrotoxicosis, thyroid hormonecoupling defect, thymic aplasia, Hurthle cell tumours of the thyroid,thyroid cancer, thyroid carcinoma, Medullary thyroid carcinoma;disorders and/or diseases of the parathyroid, such as, for example,hyperparathyroidism, hypoparathyroidism; disorders and/or diseases ofthe hypothalamus.

In addition, endocrine system and/or hormone imbalance disorders and/ordiseases may also include disorders and/or diseases of the testes orovaries, including cancer. Other disorders and/or diseases of the testesor ovaries further include, for example, ovarian cancer, polycysticovary syndrome, Klinefelter's syndrome, vanishing testes syndrome(bilateral anorchia), congenital absence of Leydig's cells,cryptorchidism, Noonan's syndrome, myotonic dystrophy, capillaryhaemangioma of the testis (benign), neoplasias of the testis andneo-testis.

Moreover, endocrine system and/or hormone imbalance disorders and/ordiseases may also include disorders and/or diseases such as, forexample, polyglandular deficiency syndromes, pheochromocytoma,neuroblastoma, multiple Endocrine neoplasia, and disorders and/orcancers of endocrine tissues.

In another embodiment, albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, maybe used to diagnose, prognose, prevent, and/or treat endocrine diseasesand/or disorders associated with the tissue(s) in which the Therapeuticprotein corresponding to the Therapeutic protein portion of the albuminprotein of the invention is expressed,

Reproductive System Disorders

The albumin fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention may be used for thediagnosis, treatment, or prevention of diseases and/or disorders of thereproductive system. Reproductive system disorders that can be treatedby the compositions of the invention, include, but are not limited to,reproductive system injuries, infections, neoplastic disorders,congenital defects, and diseases or disorders which result ininfertility, complications with pregnancy, labor, or parturition, andpostpartum difficulties.

Reproductive system disorders and/or diseases include diseases and/ordisorders of the testes, including testicular atrophy, testicularfeminization, cryptorchism (unilateral and bilateral), anorchia, ectopictestis, epididymitis and orchitis (typically resulting from infectionssuch as, for example, gonorrhea, mumps, tuberculosis, and syphilis),testicular torsion, vasitis nodosa, germ cell tumors (e.g., seminomas,embryonal cell carcinomas, teratocarcinomas, choriocarcinomas, yolk sactumors, and teratomas), stromal tumors (e.g., Leydig cell tumors),hydrocele, hematocele, varicocele, spermatocele, inguinal hernia, anddisorders of sperm production (e.g., immotile cilia syndrome, aspermia,asthenozoospermia, azoospermia, oligospermia, and teratozoospermia).

Reproductive system disorders also include disorders of the prostategland, such as acute non-bacterial prostatitis, chronic non-bacterialprostatitis, acute bacterial prostatitis, chronic bacterial prostatitis,prostatodystonia, prostatosis, granulomatous prostatitis, malacoplakia,benign prostatic hypertrophy or hyperplasia, and prostate neoplasticdisorders, including adenocarcinomas, transitional cell carcinomas,ductal carcinomas, and squamous cell carcinomas.

Additionally, the compositions of the invention may be useful in thediagnosis, treatment, and/or prevention of disorders or diseases of thepenis and urethra, including inflammatory disorders, such asbalanoposthitis, balanitis xerotica obliterans, phimosis, paraphimosis,syphilis, herpes simplex virus, gonorrhea, non-gonococcal urethritis,chlamydia, mycoplasma, trichomonas, HIV, AIDS, Reiter's syndrome,condyloma acuminatum, condyloma latum, and pearly penile papules;urethral abnormalities, such as hypospadias, epispadias, and phimosis;premalignant lesions, including Erythroplasia of Queyrat, Bowen'sdisease, Bowenoid paplosis, giant condyloma of Buscke-Lowenstein, andvarrucous carcinoma; penile cancers, including squamous cell carcinomas,carcinoma in situ, verrucous carcinoma, and disseminated penilecarcinoma; urethral neoplastic disorders, including penile urethralcarcinoma, bulbomembranous urethral carcinoma, and prostatic urethralcarcinoma; and erectile disorders, such as priapism, Peyronie's disease,erectile dysfunction, and impotence.

Moreover, diseases and/or disorders of the vas deferens includevasculititis and CBAVD (congenital bilateral absence of the vasdeferens); additionally, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be used in the diagnosis, treatment, and/or prevention of diseasesand/or disorders of the seminal vesicles, including hydatid disease,congenital chloride diarrhea, and polycystic kidney disease.

Other disorders and/or diseases of the male reproductive system include,for example, Klinefelter's syndrome, Young's syndrome, prematureejaculation, diabetes mellitus, cystic fibrosis, Kartagener's syndrome,high fever, multiple sclerosis, and gynecomastia.

Further, the polynucleotides, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beused in the diagnosis, treatment, and/or prevention of diseases and/ordisorders of the vagina and vulva, including bacterial vaginosis,candida vaginitis, herpes simplex virus, chancroid, granuloma inguinale,lymphogranuloma venereum, scabies, human papillomavirus, vaginal trauma,vulvar trauma, adenosis, chlamydia vaginitis, gonorrhea, trichomonasvaginitis, condyloma acuminatum, syphilis, molluscum contagiosum,atrophic vaginitis, Paget's disease, lichen sclerosus, lichen planus,vulvodynia, toxic shock syndrome, vaginismus, vulvovaginitis, vulvarvestibulitis, and neoplastic disorders, such as squamous cellhyperplasia, clear cell carcinoma, basal cell carcinoma, melanomas,cancer of Bartholin's gland, and vulvar intraepithelial neoplasia.

Disorders and/or diseases of the uterus include dysmenorrhea,retroverted uterus, endometriosis, fibroids, adenomyosis, anovulatorybleeding, amenorrhea, Cushing's syndrome, hydatidiform moles, Asherman'ssyndrome, premature menopause, precocious puberty, uterine polyps,dysfunctional uterine bleeding (e.g., due to aberrant hormonal signals),and neoplastic disorders, such as adenocarcinomas, keiomyosarcomas, andsarcomas. Additionally, the albumin fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionmay be useful as a marker or detector of, as well as in the diagnosis,treatment, and/or prevention of congenital uterine abnormalities, suchas bicornuate uterus, septate uterus, simple unicornuate uterus,unicornuate uterus with a noncavitary rudimentary horn, unicornuateuterus with a non-communicating cavitary rudimentary horn, unicornuateuterus with a communicating cavitary horn, arcuate uterus, uterinedidelfus, and T-shaped uterus.

Ovarian diseases and/or disorders include anovulation, polycystic ovarysyndrome (Stein-Leventhal syndrome), ovarian cysts, ovarianhypofunction, ovarian insensitivity to gonadotropins, ovarianoverproduction of androgens, right ovarian vein syndrome, amenorrhea,hirutism, and ovarian cancer (including, but not limited to, primary andsecondary cancerous growth, Sertoli-Leydig tumors, endometriod carcinomaof the ovary, ovarian papillary serous adenocarcinoma, ovarian mucinousadenocarcinoma, and Ovarian Krukenberg tumors).

Cervical diseases and/or disorders include cervicitis, chroniccervicitis, mucopurulent cervicitis, cervical dysplasia, cervicalpolyps, Nabothian cysts, cervical erosion, cervical incompetence, andcervical neoplasms (including, for example, cervical carcinoma, squamousmetaplasia, squamous cell carcinoma, adenosquamous cell neoplasia, andcolumnar cell neoplasia).

Additionally, diseases and/or disorders of the reproductive systeminclude disorders and/or diseases of pregnancy, including miscarriageand stillbirth, such as early abortion, late abortion, spontaneousabortion, induced abortion, therapeutic abortion, threatened abortion,missed abortion, incomplete abortion, complete abortion, habitualabortion, missed abortion, and septic abortion; ectopic pregnancy,anemia, Rh incompatibility, vaginal bleeding during pregnancy,gestational diabetes, intrauterine growth retardation, polyhydramnios,HELLP syndrome, abruptio placentae, placenta previa, hyperemesis,preeclampsia, eclampsia, herpes gestationis, and urticaria of pregnancy.Additionally, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention may beused in the diagnosis, treatment, and/or prevention of diseases that cancomplicate pregnancy, including heart disease, heart failure, rheumaticheart disease, congenital heart disease, mitral valve prolapse, highblood pressure, anemia, kidney disease, infectious disease (e.g.,rubella, cytomegalovirus, toxoplasmosis, infectious hepatitis,chlamydia, HIV, AIDS, and genital herpes), diabetes mellitus, Graves'disease, thyroiditis, hypothyroidism, Hashimoto's thyroiditis, chronicactive hepatitis, cirrhosis of the liver, primary biliary cirrhosis,asthma, systemic lupus eryematosis, rheumatoid arthritis, myastheniagravis, idiopathic thrombocytopenic purpura, appendicitis, ovariancysts, gallbladder disorders, and obstruction of the intestine.

Complications associated with labor and parturition include prematurerupture of the membranes, pre-term labor, post-term pregnancy,postmaturity, labor that progresses too slowly, fetal distress (e.g.,abnormal heart rate (fetal or maternal), breathing problems, andabnormal fetal position), shoulder dystocia, prolapsed umbilical cord,amniotic fluid embolism, and aberrant uterine bleeding.

Further, diseases and/or disorders of the postdelivery period, includingendometritis, myometritis, parametritis, peritonitis, pelvicthrombophlebitis, pulmonary embolism, endotoxemia, pyelonephritis,saphenous thrombophlebitis, mastitis, cystitis, postpartum hemorrhage,and inverted uterus.

Other disorders and/or diseases of the female reproductive system thatmay be diagnosed, treated, and/or prevented by the albumin fusionproteins of the invention and/or polynucleotides encoding albumin fusionproteins of the invention include, for example, Turner's syndrome,pseudohermaphroditism, premenstrual syndrome, pelvic inflammatorydisease, pelvic congestion (vascular engorgement), frigidity,anorgasmia, dyspareunia, ruptured fallopian tube, and Mittelschmerz.

Infectious Disease

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention can be used to treat or detectinfectious agents. For example, by increasing the immune response,particularly increasing the proliferation and differentiation of Band/or T cells, infectious diseases may be treated. The immune responsemay be increased by either enhancing an existing immune response, or byinitiating a new immune response. Alternatively, fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may also directly inhibit the infectious agent, withoutnecessarily eliciting an immune response.

Viruses are one example of an infectious agent that can cause disease orsymptoms that can be treated or detected by albumin fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention. Examples of viruses, include, but are not limited toExamples of viruses, include, but are not limited to the following DNAand RNA viruses and viral families: Arbovirus, Adenoviridae,Arenaviridae, Arterivirus, Birnaviridae, Bunyaviridae, Caliciviridae,Circoviridae, Coronaviridae, Dengue, EBV, HIV, Flaviviridae,Hepadnaviridae (Hepatitis), Herpesviridae (such as, Cytomegalovirus,Herpes Simplex, Herpes Zoster), Mononegavirus (e.g., Paramyxoviridae,Morbillivirus, Rhabdoviridae), Orthomyxoviridae (e.g., Influenza A,Influenza B, and parainfluenza), Papiloma virus, Papovaviridae,Parvoviridae, Picornaviridae, Poxviridae (such as Smallpox or Vaccinia),Reoviridae (e.g., Rotavirus), Retroviridae (HTLV-I, HTLV-II,Lentivirus), and Togaviridae (e.g., Rubivirus). Viruses falling withinthese families can cause a variety of diseases or symptoms, including,but not limited to: arthritis, bronchiollitis, respiratory syncytialvirus, encephalitis, eye infections (e.g., conjunctivitis, keratitis),chronic fatigue syndrome, hepatitis (A, B, C, E, Chronic Active, Delta),Japanese B encephalitis, Junin, Chikungunya, Rift Valley fever, yellowfever, meningitis, opportunistic infections (e.g., AIDS), pneumonia,Burkitt's Lymphoma, chickenpox, hemorrhagic fever, Measles, Mumps,Parainfluenza, Rabies, the common cold, Polio, leukemia, Rubella,sexually transmitted diseases, skin diseases (e.g., Kaposi's, warts),and viremia. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, canbe used to treat or detect any of these symptoms or diseases. Inspecific embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to treat: meningitis, Dengue, EBV, and/or hepatitis (e.g.,hepatitis B). In an additional specific embodiment fusion proteins ofthe invention and/or polynucleotides encoding albumin fusion proteins ofthe invention are used to treat patients nonresponsive to one or moreother commercially available hepatitis vaccines. In a further specificembodiment fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention are used to treatAIDS.

Similarly, bacterial and fungal agents that can cause disease orsymptoms and that can be treated or detected by albumin fusion proteinsof the invention and/or polynucleotides encoding albumin fusion proteinsof the invention include, but not limited to, the followingGram-Negative and Gram-positive bacteria, bacterial families, and fungi:Actinomyces (e.g., Norcardia), Acinetobacter, Cryptococcus neoformans,Aspergillus, Bacillaceae (e.g., Bacillus anthrasis), Bacteroides (e.g.,Bacteroides fragilis), Blastomycosis, Bordetella, Borrelia (e.g.,Borrelia burgdorferi), Brucella, Candidia, Campylobacter, Chlamydia,Clostridium (e.g., Clostridium botulinum, Clostridium difficile,Clostridium perfringens, Clostridium tetani), Coccidioides,Corynebacterium (e.g., Corynebacterium diptheriae), Cryptococcus,Dermatocycoses, E. coli (e.g., Enterotoxigenic E. coli andEnterohemorrhagic E. coli), Enterobacter (e.g. Enterobacter aerogenes),Enterobacteriaceae (Klebsiella, Salmonella (e.g., Salmonella typhi,Salmonella enteritidis, Salmonella typhi), Serratia, Yersinia,Shigella), Erysipelothrix, Haemophilus (e.g., Haemophilus influenza typeB), Helicobacter, Legionella (e.g., Legionella pneumophila), Leptospira,Listeria (e.g., Listeria monocytogenes), Mycoplasma, Mycobacterium(e.g., Mycobacterium leprae and Mycobacterium tuberculosis), Vibrio(e.g., Vibrio cholerae), Neisseriaceae (e.g., Neisseria gonorrhea,Neisseria meningitidis), Pasteurellacea, Proteus, Pseudomonas (e.g.,Pseudomonas aeruginosa), Rickettsiaceae, Spirochetes (e.g., Treponemaspp., Leptospira spp., Borrelia spp.), Shigella spp., Staphylococcus(e.g., Staphylococcus aureus), Meningiococcus, Pneumococcus andStreptococcus (e.g., Streptococcus pneumoniae and Groups A, B, and CStreptococci), and Ureaplasmas. These bacterial, parasitic, and fungalfamilies can cause diseases or symptoms, including, but not limited to:antibiotic-resistant infections, bacteremia, endocarditis, septicemia,eye infections (e.g., conjunctivitis), uveitis, tuberculosis,gingivitis, bacterial diarrhea, opportunistic infections (e.g., AIDSrelated infections), paronychia, prosthesis-related infections, dentalcaries, Reiter's Disease, respiratory tract infections, such as WhoopingCough or Empyema, sepsis, Lyme Disease, Cat-Scratch Disease, dysentery,paratyphoid fever, food poisoning, Legionella disease, chronic and acuteinflammation, erythema, yeast infections, typhoid, pneumonia, gonorrhea,meningitis (e.g., meningitis types A and B), chlamydia, syphilis,diphtheria, leprosy, brucellosis, peptic ulcers, anthrax, spontaneousabortions, birth defects, pneumonia, lung infections, ear infections,deafness, blindness, lethargy, malaise, vomiting, chronic diarrhea,Crohn's disease, colitis, vaginosis, sterility, pelvic inflammatorydiseases, candidiasis, paratuberculosis, tuberculosis, lupus, botulism,gangrene, tetanus, impetigo, Rheumatic Fever, Scarlet Fever, sexuallytransmitted diseases, skin diseases (e.g., cellulitis, dermatocycoses),toxemia, urinary tract infections, wound infections, noscomialinfections. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, canbe used to treat or detect any of these symptoms or diseases. Inspecific embodiments, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention areused to treat: tetanus, diptheria, botulism, and/or meningitis type B.

Moreover, parasitic agents causing disease or symptoms that can betreated, prevented, and/or diagnosed by fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventioninclude, but not limited to, the following families or class: Amebiasis,Babesiosis, Coccidiosis, Cryptosporidiosis, Dientamoebiasis, Dourine,Ectoparasitic, Giardias, Helminthiasis, Leishmaniasis, Schistisoma,Theileriasis, Toxoplasmosis, Trypanosomiasis, and Trichomonas andSporozoans (e.g., Plasmodium virax, Plasmodium falciparium, Plasmodiummalariae and Plasmodium ovale). These parasites can cause a variety ofdiseases or symptoms, including, but not limited to: Scabies,Trombiculiasis, eye infections, intestinal disease (e.g., dysentery,giardiasis), liver disease, lung disease, opportunistic infections(e.g., AIDS related), malaria, pregnancy complications, andtoxoplasmosis. Albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention, canbe used to treat, prevent, and/or diagnose any of these symptoms ordiseases. In specific embodiments, fusion proteins of the inventionand/or polynucleotides encoding albumin fusion proteins of the inventionare used to treat, prevent, and/or diagnose malaria.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention could either be byadministering an effective amount of an albumin fusion protein of theinvention to the patient, or by removing cells from the patient,supplying the cells with a polynucleotide of the present invention, andreturning the engineered cells to the patient (ex vivo therapy).Moreover, the albumin fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention can beused as an antigen in a vaccine to raise an immune response againstinfectious disease.

Regeneration

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention can be used to differentiate,proliferate, and attract cells, leading to the regeneration of tissues.(See, Science 276:59-87 (1997)). The regeneration of tissues could beused to repair, replace, or protect tissue damaged by congenitaldefects, trauma (wounds, burns, incisions, or ulcers), age, disease(e.g. osteoporosis, osteocarthritis, periodontal disease, liverfailure), surgery, including cosmetic plastic surgery, fibrosis,reperfusion injury, or systemic cytokine damage.

Tissues that could be regenerated using the present invention includeorgans (e.g., pancreas, liver, intestine, kidney, skin, endothelium),muscle (smooth, skeletal or cardiac), vasculature (including vascularand lymphatics), nervous, hematopoietic, and skeletal (bone, cartilage,tendon, and ligament) tissue. Preferably, regeneration occurs without ordecreased scarring. Regeneration also may include angiogenesis.

Moreover, fusion proteins of the invention and/or polynucleotidesencoding albumin fusion proteins of the invention, may increaseregeneration of tissues difficult to heal. For example, increasedtendon/ligament regeneration would quicken recovery time after damage.Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention could also be usedprophylactically in an effort to avoid damage. Specific diseases thatcould be treated include of tendinitis, carpal tunnel syndrome, andother tendon or ligament defects. A further example of tissueregeneration of non-healing wounds includes pressure ulcers, ulcersassociated with vascular insufficiency, surgical, and traumatic wounds.

Similarly, nerve and brain tissue could also be regenerated by usingfusion proteins of the invention and/or polynucleotides encoding albuminfusion proteins of the invention, to proliferate and differentiate nervecells. Diseases that could be treated using this method include centraland peripheral nervous system diseases, neuropathies, or mechanical andtraumatic disorders (e.g., spinal cord disorders, head trauma,cerebrovascular disease, and stoke). Specifically, diseases associatedwith peripheral nerve injuries, peripheral neuropathy (e.g., resultingfrom chemotherapy or other medical therapies), localized neuropathies,and central nervous system diseases (e.g., Alzheimer's disease,Parkinson's disease, Huntington's disease, amyotrophic lateralsclerosis, and Shy-Drager syndrome), could all be treated using thealbumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention.

Gastrointestinal Disorders

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention, may be used to treat, prevent,diagnose, and/or prognose gastrointestinal disorders, includinginflammatory diseases and/or conditions, infections, cancers (e.g.,intestinal neoplasms (carcinoid tumor of the small intestine,non-Hodgkin's lymphoma of the small intestine, small bowl lymphoma)),and ulcers, such as peptic ulcers.

Gastrointestinal disorders include dysphagia, odynophagia, inflammationof the esophagus, peptic esophagitis, gastric reflux, submucosalfibrosis and stricturing, Mallory-Weiss lesions, leiomyomas, lipomas,epidermal cancers, adeoncarcinomas, gastric retention disorders,gastroenteritis, gastric atrophy, gastric/stomach cancers, polyps of thestomach, autoimmune disorders such as pernicious anemia, pyloricstenosis, gastritis (bacterial, viral, eosinophilic, stress-induced,chronic erosive, atrophic, plasma cell, and Menetrier's), and peritonealdiseases (e.g., chyloperioneum, hemoperitoneum, mesenteric cyst,mesenteric lymphadenitis, mesenteric vascular occlusion, panniculitis,neoplasms, peritonitis, pneumoperitoneum, bubphrenic abscess,).

Gastrointestinal disorders also include disorders associated with thesmall intestine, such as malabsorption syndromes, distension, irritablebowel syndrome, sugar intolerance, celiac disease, duodenal ulcers,duodenitis, tropical sprue, Whipple's disease, intestinallymphangiectasia, Crohn's disease, appendicitis, obstructions of theileum, Meckel's diverticulum, multiple diverticula, failure of completerotation of the small and large intestine, lymphoma, and bacterial andparasitic diseases (such as Traveler's diarrhea, typhoid andparatyphoid, cholera, infection by Roundworms (Ascariasis lumbricoides),Hookworms (Ancylostoma duodenale), Threadworms (Enterobiusvermicularis), Tapeworms (Taenia saginata, Echinococcus granulosus,Diphyllobothrium spp., and T. solium).

Liver diseases and/or disorders include intrahepatic cholestasis(alagille syndrome, biliary liver cirrhosis), fatty liver (alcoholicfatty liver, reye syndrome), hepatic vein thrombosis, hepatolentriculardegeneration, hepatomegaly, hepatopulmonary syndrome, hepatorenalsyndrome, portal hypertension (esophageal and gastric varices), liverabscess (amebic liver abscess), liver cirrhosis (alcoholic, biliary andexperimental), alcoholic liver diseases (fatty liver, hepatitis,cirrhosis), parasitic (hepatic echinococcosis, fascioliasis, amebicliver abscess), jaundice (hemolytic, hepatocellular, and cholestatic),cholestasis, portal hypertension, liver enlargement, ascites, hepatitis(alcoholic hepatitis, animal hepatitis, chronic hepatitis (autoimmune,hepatitis B, hepatitis C, hepatitis D, drug induced), toxic hepatitis,viral human hepatitis (hepatitis A, hepatitis B, hepatitis C, hepatitisD, hepatitis E), Wilson's disease, granulomatous hepatitis, secondarybiliary cirrhosis, hepatic encephalopathy, portal hypertension, varices,hepatic encephalopathy, primary biliary cirrhosis, primary sclerosingcholangitis, hepatocellular adenoma, hemangiomas, bile stones, liverfailure (hepatic encephalopathy, acute liver failure), and liverneoplasms (angiomyolipoma, calcified liver metastases, cystic livermetastases, epithelial tumors, fibrolamellar hepatocarcinoma, focalnodular hyperplasia, hepatic adenoma, hepatobiliary cystadenoma,hepatoblastoma, hepatocellular carcinoma, hepatoma, liver cancer, liverhemangioendothelioma, mesenchymal hamartoma, mesenchymal tumors ofliver, nodular regenerative hyperplasia, benign liver tumors (Hepaticcysts [Simple cysts, Polycystic liver disease, Hepatobiliarycystadenoma, Choledochal cyst], Mesenchymal tumors [Mesenchymalhamartoma, Infantile hemangioendothelioma, Hemangioma, Peliosis hepatis,Lipomas, Inflammatory pseudotumor, Miscellaneous], Epithelial tumors[Bile duct epithelium (Bile duct hamartoma, Bile duct adenoma),Hepatocyte (Adenoma, Focal nodular hyperplasia, Nodular regenerativehyperplasia)], malignant liver tumors [hepatocellular, hepatoblastoma,hepatocellular carcinoma, cholangiocellular, cholangiocarcinoma,cystadenocarcinoma, tumors of blood vessels, angiosarcoma, Karposi'ssarcoma, hemangioendothelioma, other tumors, embryonal sarcoma,fibrosarcoma, leiomyosarcoma, rhabdomyosarcoma, carcinosarcoma,teratoma, carcinoid, squamous carcinoma, primary lymphoma]), peliosishepatis, erythrohepatic porphyria, hepatic porphyria (acute intermittentporphyria, porphyria cutanea tarda), Zellweger syndrome).

Pancreatic diseases and/or disorders include acute pancreatitis, chronicpancreatitis (acute necrotizing pancreatitis, alcoholic pancreatitis),neoplasms (adenocarcinoma of the pancreas, cystadenocarcinoma,insulinoma, gastrinoma, and glucagonoma, cystic neoplasms, islet-celltumors, pancreoblastoma), and other pancreatic diseases (e.g., cysticfibrosis, cyst (pancreatic pseudocyst, pancreatic fistula,insufficiency)).

Gallbladder diseases include gallstones (cholelithiasis andcholedocholithiasis), postcholecystectomy syndrome, diverticulosis ofthe gallbladder, acute cholecystitis, chronic cholecystitis, bile ducttumors, and mucocele.

Diseases and/or disorders of the large intestine includeantibiotic-associated colitis, diverticulitis, ulcerative colitis,acquired megacolon, abscesses, fungal and bacterial infections,anorectal disorders (e.g., fissures, hemorrhoids), colonic diseases(colitis, colonic neoplasms [colon cancer, adenomatous colon polyps(e.g., villous adenoma), colon carcinoma, colorectal cancer], colonicdiverticulitis, colonic diverticulosis, megacolon [Hirschsprung disease,toxic megacolon]; sigmoid diseases [proctocolitis, sigmoin neoplasms]),constipation, Crohn's disease, diarrhea (infantile diarrhea, dysentery),duodenal diseases (duodenal neoplasms, duodenal obstruction, duodenalulcer, duodenitis), enteritis (enterocolitis), HIV enteropathy, ilealdiseases (ileal neoplasms, ileitis), immunoproliferative smallintestinal disease, inflammatory bowel disease (ulcerative colitis,Crohn's disease), intestinal atresia, parasitic diseases (anisakiasis,balantidiasis, blastocystis infections, cryptosporidiosis,dientamoebiasis, amebic dysentery, giardiasis), intestinal fistula(rectal fistula), intestinal neoplasms (cecal neoplasms, colonicneoplasms, duodenal neoplasms, ileal neoplasms, intestinal polyps,jejunal neoplasms, rectal neoplasms), intestinal obstruction (afferentloop syndrome, duodenal obstruction, impacted feces, intestinalpseudo-obstruction [cecal volvulus], intussusception), intestinalperforation, intestinal polyps (colonic polyps, gardner syndrome,peutz-jeghers syndrome), jejunal diseases (jejunal neoplasms),malabsorption syndromes (blind loop syndrome, celiac disease, lactoseintolerance, short bowl syndrome, tropical sprue, whipple's disease),mesenteric vascular occlusion, pneumatosis cystoides intestinalis,protein-losing enteropathies (intestinal lymphagiectasis), rectaldiseases (anus diseases, fecal incontinence, hemorrhoids, proctitis,rectal fistula, rectal prolapse, rectocele), peptic ulcer (duodenalulcer, peptic esophagitis, hemorrhage, perforation, stomach ulcer,Zollinger-Ellison syndrome), postgastrectomy syndromes (dumpingsyndrome), stomach diseases (e.g., achlorhydria, duodenogastric reflux(bile reflux), gastric antral vascular ectasia, gastric fistula, gastricoutlet obstruction, gastritis (atrophic or hypertrophic), gastroparesis,stomach dilatation, stomach diverticulum, stomach neoplasms (gastriccancer, gastric polyps, gastric adenocarcinoma, hyperplastic gastricpolyp), stomach rupture, stomach ulcer, stomach volvulus), tuberculosis,visceroptosis, vomiting (e.g., hematemesis, hyperemesis gravidarum,postoperative nausea and vomiting) and hemorrhagic colitis.

Further diseases and/or disorders of the gastrointestinal system includebiliary tract diseases, such as, gastroschisis, fistula (e.g., biliaryfistula, esophageal fistula, gastric fistula, intestinal fistula,pancreatic fistula), neoplasms (e.g., biliary tract neoplasms,esophageal neoplasms, such as adenocarcinoma of the esophagus,esophageal squamous cell carcinoma, gastrointestinal neoplasms,pancreatic neoplasms, such as adenocarcinoma of the pancreas, mucinouscystic neoplasm of the pancreas, pancreatic cystic neoplasms,pancreatoblastoma, and peritoneal neoplasms), esophageal disease (e.g.,bullous diseases, candidiasis, glycogenic acanthosis, ulceration,barrett esophagus varices, atresia, cyst, diverticulum (e.g., Zenker'sdiverticulum), fistula (e.g., tracheoesophageal fistula), motilitydisorders (e.g., CREST syndrome, deglutition disorders, achalasia,spasm, gastroesophageal reflux), neoplasms, perforation (e.g., Boerhaavesyndrome, Mallory-Weiss syndrome), stenosis, esophagitis, diaphragmatichernia (e.g., hiatal hernia); gastrointestinal diseases, such as,gastroenteritis (e.g., cholera morbus, norwalk virus infection),hemorrhage (e.g., hematemesis, melena, peptic ulcer hemorrhage), stomachneoplasms (gastric cancer, gastric polyps, gastric adenocarcinoma,stomach cancer)), hernia (e.g., congenital diaphragmatic hernia, femoralhernia, inguinal hernia, obturator hernia, umbilical hernia, ventralhernia), and intestinal diseases (e.g., cecal diseases (appendicitis,cecal neoplasms)).

Chemotaxis

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may have chemotaxis activity. Achemotaxic molecule attracts or mobilizes cells (e.g., monocytes,fibroblasts, neutrophils, T-cells, mast cells, eosinophils, epithelialand/or endothelial cells) to a particular site in the body, such asinflammation, infection, or site of hyperproliferation. The mobilizedcells can then fight off and/or heal the particular trauma orabnormality.

Albumin fusion proteins of the invention and/or polynucleotides encodingalbumin fusion proteins of the invention may increase chemotaxicactivity of particular cells. These chemotactic molecules can then beused to treat inflammation, infection, hyperproliferative disorders, orany immune system disorder by increasing the number of cells targeted toa particular location in the body. For example, chemotaxic molecules canbe used to treat wounds and other trauma to tissues by attracting immunecells to the injured location. Chemotactic molecules of the presentinvention can also attract fibroblasts, which can be used to treatwounds.

It is also contemplated that fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention mayinhibit chemotactic activity. These molecules could also be used totreat disorders. Thus, fusion proteins of the invention and/orpolynucleotides encoding albumin fusion proteins of the invention couldbe used as an inhibitor of chemotaxis.

Binding Activity

Albumin fusion proteins of the invention may be used to screen formolecules that bind to the Therapeutic protein portion of the fusionprotein or for molecules to which the Therapeutic protein portion of thefusion protein binds. The binding of the fusion protein and the moleculemay activate (agonist), increase, inhibit (antagonist), or decreaseactivity of the fusion protein or the molecule bound. Examples of suchmolecules include antibodies, oligonucleotides, proteins (e.g.,receptors), or small molecules.

Preferably, the molecule is closely related to the natural ligand of theTherapeutic protein portion of the fusion protein of the invention,e.g., a fragment of the ligand, or a natural substrate, a ligand, astructural or functional mimetic. (See, Coligan et al., CurrentProtocols in Immunology 1(2):Chapter 5 (1991)). Similarly, the moleculecan be closely related to the natural receptor to which the Therapeuticprotein portion of an albumin fusion protein of the invention binds, orat least, a fragment of the receptor capable of being bound by theTherapeutic protein portion of an albumin fusion protein of theinvention (e.g., active site). In either case, the molecule can berationally designed using known techniques.

Preferably, the screening for these molecules involves producingappropriate cells which express the albumin fusion proteins of theinvention. Preferred cells include cells from mammals, yeast,Drosophila, or E. coli.

The assay may simply test binding of a candidate compound to an albuminfusion protein of the invention, wherein binding is detected by a label,or in an assay involving competition with a labeled competitor. Further,the assay may test whether the candidate compound results in a signalgenerated by binding to the fusion protein.

Alternatively, the assay can be carried out using cell-freepreparations, fusion protein/molecule affixed to a solid support,chemical libraries, or natural product mixtures. The assay may alsosimply comprise the steps of mixing a candidate compound with a solutioncontaining an albumin fusion protein, measuring fusion protein/moleculeactivity or binding, and comparing the fusion protein/molecule activityor binding to a standard.

Preferably, an ELISA assay can measure fusion protein level or activityin a sample (e.g., biological sample) using a monoclonal or polyclonalantibody. The antibody can measure fusion protein level or activity byeither binding, directly or indirectly, to the albumin fusion protein orby competing with the albumin fusion protein for a substrate.

Additionally, the receptor to which a Therapeutic protein portion of analbumin fusion protein of the invention binds can be identified bynumerous methods known to those of skill in the art, for example, ligandpanning and FACS sorting (Coligan, et al., Current Protocols in Immun.,1(2), Chapter 5, (1991)). For example, in cases wherein the Therapeuticprotein portion of the fusion protein corresponds to FGF, expressioncloning may be employed wherein polyadenylated RNA is prepared from acell responsive to the albumin fusion protein, for example, NIH3T3 cellswhich are known to contain multiple receptors for the FGF familyproteins, and SC-3 cells, and a cDNA library created from this RNA isdivided into pools and used to transfect COS cells or other cells thatare not responsive to the albumin fusion protein. Transfected cellswhich are grown on glass slides are exposed to the albumin fusionprotein of the present invention, after they have been labeled. Thealbumin fusion proteins can be labeled by a variety of means includingiodination or inclusion of a recognition site for a site-specificprotein kinase.

Following fixation and incubation, the slides are subjected toauto-radiographic analysis. Positive pools are identified and sub-poolsare prepared and re-transfected using an iterative sub-pooling andre-screening process, eventually yielding a single clones that encodesthe putative receptor.

As an alternative approach for receptor identification, a labeledalbumin fusion protein can be photoaffinity linked with cell membrane orextract preparations that express the receptor molecule for theTherapeutic protein component of an albumin fusion protein of theinvention, the linked material may be resolved by PAGE analysis andexposed to X-ray film. The labeled complex containing the receptors ofthe fusion protein can be excised, resolved into peptide fragments, andsubjected to protein microsequencing. The amino acid sequence obtainedfrom microsequencing would be used to design a set of degenerateoligonucleotide probes to screen a cDNA library to identify the genesencoding the putative receptors.

Moreover, the techniques of gene-shuffling, motif-shuffling,exon-shuffling, and/or codon-shuffling (collectively referred to as “DNAshuffling”) may be employed to modulate the activities of the fusionprotein, and/or Therapeutic protein portion or albumin component of analbumin fusion protein of the present invention, thereby effectivelygenerating agonists and antagonists of an albumin fusion protein of thepresent invention. See generally, U.S. Pat. Nos. 5,605,793, 5,811,238,5,830,721, 5,834,252, and 5,837,458, and Patten, P. A., et al., Curr.Opinion Biotechnol. 8:724-33 (1997); Harayama, S. Trends Biotechnol.16(2):76-82 (1998); Hansson, L. O., et al., J. Mol. Biol. 287:265-76(1999); and Lorenzo, M. M. and Blasco, R. Biotechniques 24(2):308-13(1998); each of these patents and publications are hereby incorporatedby reference). In one embodiment, alteration of polynucleotides encodingalbumin fusion proteins of the invention and thus, the albumin fusionproteins encoded thereby, may be achieved by DNA shuffling. DNAshuffling involves the assembly of two or more DNA segments into adesired molecule by homologous, or site-specific, recombination. Inanother embodiment, polynucleotides encoding albumin fusion proteins ofthe invention and thus, the albumin fusion proteins encoded thereby, maybe altered by being subjected to random mutagenesis by error-prone PCR,random nucleotide insertion or other methods prior to recombination. Inanother embodiment, one or more components, motifs, sections, parts,domains, fragments, etc., of an albumin fusion protein of the presentinvention may be recombined with one or more components, motifs,sections, parts, domains, fragments, etc. of one or more heterologousmolecules. In preferred embodiments, the heterologous molecules arefamily members. In further preferred embodiments, the heterologousmolecule is a growth factor such as, for example, platelet-derivedgrowth factor (PDGF), insulin-like growth factor (IGF-I), transforminggrowth factor (TGF)-alpha, epidermal growth factor (EGF), fibroblastgrowth factor (FGF), TGF-beta, bone morphogenetic protein (BMP)-2,BMP-4, BMP-5, BMP-6, BMP-7, activins A and B, decapentaplegic (dpp),60A, OP-2, dorsalin, growth differentiation factors (GDFs), nodal, MIS,inhibin-alpha, TGF-beta1, TGF-beta2, TGF-beta3, TGF-beta5, andglial-derived neurotrophic factor (GDNF).

Other preferred fragments are biologically active fragments of theTherapeutic protein portion and/or albumin component of the albuminfusion proteins of the present invention. Biologically active fragmentsare those exhibiting activity similar, but not necessarily identical, toan activity of a Therapeutic protein portion and/or albumin component ofthe albumin fusion proteins of the present invention. The biologicalactivity of the fragments may include an improved desired activity, or adecreased undesirable activity.

Additionally, this invention provides a method of screening compounds toidentify those which modulate the action of an albumin fusion protein ofthe present invention. An example of such an assay comprises combining amammalian fibroblast cell, an albumin fusion protein of the presentinvention, and the compound to be screened and ³[H] thymidine under cellculture conditions where the fibroblast cell would normally proliferate.A control assay may be performed in the absence of the compound to bescreened and compared to the amount of fibroblast proliferation in thepresence of the compound to determine if the compound stimulatesproliferation by determining the uptake of ³[H] thymidine in each case.The amount of fibroblast cell proliferation is measured by liquidscintillation chromatography which measures the incorporation of ³[H]thymidine. Both agonist and antagonist compounds may be identified bythis procedure.

In another method, a mammalian cell or membrane preparation expressing areceptor for the Therapeutic protein component of a fusion protine ofthe invention is incubated with a labeled fusion protein of the presentinvention in the presence of the compound. The ability of the compoundto enhance or block this interaction could then be measured.Alternatively, the response of a known second messenger system followinginteraction of a compound to be screened and the receptor is measuredand the ability of the compound to bind to the receptor and elicit asecond messenger response is measured to determine if the compound is apotential fusion protein. Such second messenger systems include but arenot limited to, cAMP guanylate cyclase, ion channels or phosphoinositidehydrolysis.

All of these above assays can be used as diagnostic or prognosticmarkers. The molecules discovered using these assays can be used totreat disease or to bring about a particular result in a patient (e.g.,blood vessel growth) by activating or inhibiting the fusionprotein/molecule. Moreover, the assays can discover agents which mayinhibit or enhance the production of the albumin fusion proteins of theinvention from suitably manipulated cells or tissues.

Therefore, the invention includes a method of identifying compoundswhich bind to an albumin fusion protein of the invention comprising thesteps of: (a) incubating a candidate binding compound with an albuminfusion protein of the present invention; and (b) determining if bindinghas occurred. Moreover, the invention includes a method of identifyingagonists/antagonists comprising the steps of: (a) incubating a candidatecompound with an albumin fusion protein of the present invention, (b)assaying a biological activity, and (b) determining if a biologicalactivity of the fusion protein has been altered.

Targeted Delivery

In another embodiment, the invention provides a method of deliveringcompositions to targeted cells expressing a receptor for a component ofan albumin fusion protein of the invention.

As discussed herein, fusion proteins of the invention may be associatedwith heterologous polypeptides, heterologous nucleic acids, toxins, orprodrugs via hydrophobic, hydrophilic, ionic and/or covalentinteractions. In one embodiment, the invention provides a method for thespecific delivery of compositions of the invention to cells byadministering fusion proteins of the invention (including antibodies)that are associated with heterologous polypeptides or nucleic acids. Inone example, the invention provides a method for delivering aTherapeutic protein into the targeted cell. In another example, theinvention provides a method for delivering a single stranded nucleicacid (e.g., antisense or ribozymes) or double stranded nucleic acid(e.g., DNA that can integrate into the cell's genome or replicateepisomally and that can be transcribed) into the targeted cell.

In another embodiment, the invention provides a method for the specificdestruction of cells (e.g., the destruction of tumor cells) byadministering an albumin fusion protein of the invention (e.g.,polypeptides of the invention or antibodies of the invention) inassociation with toxins or cytotoxic prodrugs.

By “toxin” is meant compounds that bind and activate endogenouscytotoxic effector systems, radioisotopes, holotoxins, modified toxins,catalytic subunits of toxins, or any molecules or enzymes not normallypresent in or on the surface of a cell that under defined conditionscause the cell's death. Toxins that may be used according to the methodsof the invention include, but are not limited to, radioisotopes known inthe art, compounds such as, for example, antibodies (or complementfixing containing portions thereof) that bind an inherent or inducedendogenous cytotoxic effector system, thymidine kinase, endonuclease,RNAse, alpha toxin, ricin, abrin, Pseudomonas exotoxin A, diphtheriatoxin, saporin, momordin, gelonin, pokeweed antiviral protein,alpha-sarcin and cholera toxin. By “cytotoxic prodrug” is meant anon-toxic compound that is converted by an enzyme, normally present inthe cell, into a cytotoxic compound. Cytotoxic prodrugs that may be usedaccording to the methods of the invention include, but are not limitedto, glutamyl derivatives of benzoic acid mustard alkylating agent,phosphate derivatives of etoposide or mitomycin C, cytosine arabinoside,daunorubisin, and phenoxyacetamide derivatives of doxorubicin.

Drug Screening

Further contemplated is the use of the albumin fusion proteins of thepresent invention, or the polynucleotides encoding these fusionproteins, to screen for molecules which modify the activities of thealbumin fusion protein of the present invention or proteinscorresponding to the Therapeutic protein portion of the albumin fusionprotein. Such a method would include contacting the fusion protein witha selected compound(s) suspected of having antagonist or agonistactivity, and assaying the activity of the fusion protein followingbinding.

This invention is particularly useful for screening therapeuticcompounds by using the albumin fusion proteins of the present invention,or binding fragments thereof, in any of a variety of drug screeningtechniques. The albumin fusion protein employed in such a test may beaffixed to a solid support, expressed on a cell surface, free insolution, or located intracellularly. One method of drug screeningutilizes eukaryotic or prokaryotic host cells which are stablytransformed with recombinant nucleic acids expressing the albumin fusionprotein. Drugs are screened against such transformed cells orsupernatants obtained from culturing such cells, in competitive bindingassays. One may measure, for example, the formulation of complexesbetween the agent being tested and an albumin fusion protein of thepresent invention.

Thus, the present invention provides methods of screening for drugs orany other agents which affect activities mediated by the albumin fusionproteins of the present invention. These methods comprise contactingsuch an agent with an albumin fusion protein of the present invention ora fragment thereof and assaying for the presence of a complex betweenthe agent and the albumin fusion protein or a fragment thereof, bymethods well known in the art. In such a competitive binding assay, theagents to screen are typically labeled. Following incubation, free agentis separated from that present in bound form, and the amount of free oruncomplexed label is a measure of the ability of a particular agent tobind to the albumin fusion protein of the present invention.

Another technique for drug screening provides high throughput screeningfor compounds having suitable binding affinity to an albumin fusionprotein of the present invention, and is described in great detail inEuropean Patent Application 84/03564, published on Sep. 13, 1984, whichis incorporated herein by reference herein. Briefly stated, largenumbers of different small peptide test compounds are synthesized on asolid substrate, such as plastic pins or some other surface. The peptidetest compounds are reacted with an albumin fusion protein of the presentinvention and washed. Bound peptides are then detected by methods wellknown in the art. Purified albumin fusion protein may be coated directlyonto plates for use in the aforementioned drug screening techniques. Inaddition, non-neutralizing antibodies may be used to capture the peptideand immobilize it on the solid support.

This invention also contemplates the use of competitive drug screeningassays in which neutralizing antibodies capable of binding an albuminfusion protein of the present invention specifically compete with a testcompound for binding to the albumin fusion protein or fragments thereof.In this manner, the antibodies are used to detect the presence of anypeptide which shares one or more antigenic epitopes with an albuminfusion protein of the invention.

Binding Peptides and Other Molecules

The invention also encompasses screening methods for identifyingpolypeptides and nonpolypeptides that bind albumin fusion proteins ofthe invention, and the binding molecules identified thereby. Thesebinding molecules are useful, for example, as agonists and antagonistsof the albumin fusion proteins of the invention. Such agonists andantagonists can be used, in accordance with the invention, in thetherapeutic embodiments described in detail, below.

This method comprises the steps of:

-   -   contacting an albumin fusion protein of the invention with a        plurality of molecules; and    -   identifying a molecule that binds the albumin fusion protein.

The step of contacting the albumin fusion protein of the invention withthe plurality of molecules may be effected in a number of ways. Forexample, one may contemplate immobilizing the albumin fusion protein ona solid support and bringing a solution of the plurality of molecules incontact with the immobilized polypeptides. Such a procedure would beakin to an affinity chromatographic process, with the affinity matrixbeing comprised of the immobilized albumin fusion protein of theinvention. The molecules having a selective affinity for the albuminfusion protein can then be purified by affinity selection. The nature ofthe solid support, process for attachment of the albumin fusion proteinto the solid support, solvent, and conditions of the affinity isolationor selection are largely conventional and well known to those ofordinary skill in the art.

Alternatively, one may also separate a plurality of polypeptides intosubstantially separate fractions comprising a subset of or individualpolypeptides. For instance, one can separate the plurality ofpolypeptides by gel electrophoresis, column chromatography, or likemethod known to those of ordinary skill for the separation ofpolypeptides. The individual polypeptides can also be produced by atransformed host cell in such a way as to be expressed on or about itsouter surface (e.g., a recombinant phage). Individual isolates can thenbe “probed” by an albumin fusion protein of the invention, optionally inthe presence of an inducer should one be required for expression, todetermine if any selective affinity interaction takes place between thealbumin fusion protein and the individual clone. Prior to contacting thealbumin fusion protein with each fraction comprising individualpolypeptides, the polypeptides could first be transferred to a solidsupport for additional convenience. Such a solid support may simply be apiece of filter membrane, such as one made of nitrocellulose or nylon.In this manner, positive clones could be identified from a collection oftransformed host cells of an expression library, which harbor a DNAconstruct encoding a polypeptide having a selective affinity for analbumin fusion protein of the invention. Furthermore, the amino acidsequence of the polypeptide having a selective affinity for an albuminfusion protein of the invention can be determined directly byconventional means or the coding sequence of the DNA encoding thepolypeptide can frequently be determined more conveniently. The primarysequence can then be deduced from the corresponding DNA sequence. If theamino acid sequence is to be determined from the polypeptide itself, onemay use microsequencing techniques. The sequencing technique may includemass spectroscopy.

In certain situations, it may be desirable to wash away any unboundpolypeptides from a mixture of an albumin fusion protein of theinvention and the plurality of polypeptides prior to attempting todetermine or to detect the presence of a selective affinity interaction.Such a wash step may be particularly desirable when the albumin fusionprotein of the invention or the plurality of polypeptides are bound to asolid support.

The plurality of molecules provided according to this method may beprovided by way of diversity libraries, such as random or combinatorialpeptide or nonpeptide libraries which can be screened for molecules thatspecifically bind an albumin fusion protein of the invention. Manylibraries are known in the art that can be used, e.g., chemicallysynthesized libraries, recombinant (e.g., phage display libraries), andin vitro translation-based libraries. Examples of chemically synthesizedlibraries are described in Fodor et al., Science 251:767-773 (1991);Houghten et al., Nature 354:84-86 (1991); Lam et al., Nature 354:82-84(1991); Medynski, Bio/Technology 12:709-710 (1994); Gallop et al., J.Medicinal Chemistry 37(9):1233-1251 (1994); Ohlmeyer et al., Proc. Natl.Acad. Sci. USA 90:10922-10926 (1993); Erb et al., Proc. Natl. Acad. Sci.USA 91:11422-11426 (1994); Houghten et al., Biotechniques 13:412 (1992);Jayawickreme et al., Proc. Natl. Acad. Sci. USA 91:1614-1618 (1994);Salmon et al., Proc. Natl. Acad. Sci. USA 90:11708-11712 (1993); PCTPublication No. WO 93/20242; and Brenner and Lerner, Proc. Natl. Acad.Sci. USA 89:5381-5383 (1992).

Examples of phage display libraries are described in Scott et al.,Science 249:386-390 (1990); Devlin et al., Science, 249:404-406 (1990);Christian et al., 1992, J. Mol. Biol. 227:711-718 1992); Lenstra, J.Immunol. Meth. 152:149-157 (1992); Kay et al., Gene 128:59-65 (1993);and PCT Publication No. WO 94/18318 dated Aug. 18, 1994.

In vitro translation-based libraries include but are not limited tothose described in PCT Publication No. WO 91/05058 dated Apr. 18, 1991;and Mattheakis et al., Proc. Natl. Acad. Sci. USA 91:9022-9026 (1994).

By way of examples of nonpeptide libraries, a benzodiazepine library(see e.g., Bunin et al., Proc. Natl. Acad. Sci. USA 91:4708-4712 (1994))can be adapted for use. Peptoid libraries (Simon et al., Proc. Natl.Acad. Sci. USA 89:9367-9371 (1992)) can also be used. Another example ofa library that can be used, in which the amide functionalities inpeptides have been permethylated to generate a chemically transformedcombinatorial library, is described by Ostresh et al. (Proc. Natl. Acad.Sci. USA 91:11138-11142 (1994)).

The variety of non-peptide libraries that are useful in the presentinvention is great. For example, Ecker and Crooke (Bio/Technology13:351-360 (1995) list benzodiazepines, hydantoins, piperazinediones,biphenyls, sugar analogs, beta-mercaptoketones, arylacetic acids,acylpiperidines, benzopyrans, cubanes, xanthines, aminimides, andoxazolones as among the chemical species that form the basis of variouslibraries.

Non-peptide libraries can be classified broadly into two types:decorated monomers and oligomers. Decorated monomer libraries employ arelatively simple scaffold structure upon which a variety functionalgroups is added. Often the scaffold will be a molecule with a knownuseful pharmacological activity. For example, the scaffold might be thebenzodiazepine structure.

Non-peptide oligomer libraries utilize a large number of monomers thatare assembled together in ways that create new shapes that depend on theorder of the monomers. Among the monomer units that have been used arecarbamates, pyrrolinones, and morpholinos. Peptoids, peptide-likeoligomers in which the side chain is attached to the alpha amino grouprather than the alpha carbon, form the basis of another version ofnon-peptide oligomer libraries. The first non-peptide oligomer librariesutilized a single type of monomer and thus contained a repeatingbackbone. Recent libraries have utilized more than one monomer, givingthe libraries added flexibility.

Screening the libraries can be accomplished by any of a variety ofcommonly known methods. See, e.g., the following references, whichdisclose screening of peptide libraries: Parmley et al., Adv. Exp. Med.Biol. 251:215-218 (1989); Scott et al., Science 249:386-390 (1990);Fowlkes et al., BioTechniques 13:422-427 (1992); Oldenburg et al., Proc.Natl. Acad. Sci. USA 89:5393-5397 (1992); Yu et al., Cell 76:933-945(1994); Staudt et al., Science 241:577-580 (1988); Bock et al., Nature355:564-566 (1992); Tuerk et al., Proc. Natl. Acad. Sci. USA89:6988-6992 (1992); Ellington et al., Nature 355:850-852 (1992); U.S.Pat. No. 5,096,815, U.S. Pat. No. 5,223,409, and U.S. Pat. No.5,198,346, all to Ladner et al.; Rebar et al., Science 263:671-673(1993); and PCT Publication No. WO 94/18318.

In a specific embodiment, screening to identify a molecule that binds analbumin fusion protein of the invention can be carried out by contactingthe library members with an albumin fusion protein of the inventionimmobilized on a solid phase and harvesting those library members thatbind to the albumin fusion protein. Examples of such screening methods,termed “panning” techniques are described by way of example in Parmleyet al., Gene 73:305-318 (1988); Fowlkes et al., BioTechniques 13:422-427(1992); PCT Publication No. WO 94/18318; and in references cited herein.

In another embodiment, the two-hybrid system for selecting interactingproteins in yeast (Fields et al., Nature 340:245-246 (1989); Chien etal., Proc. Natl. Acad. Sci. USA 88:9578-9582 (1991) can be used toidentify molecules that specifically bind to polypeptides of theinvention.

Where the binding molecule is a polypeptide, the polypeptide can beconveniently selected from any peptide library, including random peptidelibraries, combinatorial peptide libraries, or biased peptide libraries.The term “biased” is used herein to mean that the method of generatingthe library is manipulated so as to restrict one or more parameters thatgovern the diversity of the resulting collection of molecules, in thiscase peptides.

Thus, a truly random peptide library would generate a collection ofpeptides in which the probability of finding a particular amino acid ata given position of the peptide is the same for all 20 amino acids. Abias can be introduced into the library, however, by specifying, forexample, that a lysine occur every fifth amino acid or that positions 4,8, and 9 of a decapeptide library be fixed to include only arginine.Clearly, many types of biases can be contemplated, and the presentinvention is not restricted to any particular bias. Furthermore, thepresent invention contemplates specific types of peptide libraries, suchas phage displayed peptide libraries and those that utilize a DNAconstruct comprising a lambda phage vector with a DNA insert.

As mentioned above, in the case of a binding molecule that is apolypeptide, the polypeptide may have about 6 to less than about 60amino acid residues, preferably about 6 to about 10 amino acid residues,and most preferably, about 6 to about 22 amino acids. In anotherembodiment, a binding polypeptide has in the range of 15-100 aminoacids, or 20-50 amino acids.

The selected binding polypeptide can be obtained by chemical synthesisor recombinant expression.

Other Activities

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention, may be employed intreatment for stimulating re-vascularization of ischemic tissues due tovarious disease conditions such as thrombosis, arteriosclerosis, andother cardiovascular conditions. The albumin fusion proteins of theinvention and/or polynucleotides encoding albumin fusion proteins of theinvention may also be employed to stimulate angiogenesis and limbregeneration, as discussed above.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be employedfor treating wounds due to injuries, burns, post-operative tissuerepair, and ulcers since they are mitogenic to various cells ofdifferent origins, such as fibroblast cells and skeletal muscle cells,and therefore, facilitate the repair or replacement of damaged ordiseased tissue.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be employedstimulate neuronal growth and to treat and prevent neuronal damage whichoccurs in certain neuronal disorders or neuro-degenerative conditionssuch as Alzheimer's disease, Parkinson's disease, and AIDS-relatedcomplex. An albumin fusion protein of the invention and/orpolynucleotide encoding an albumin fusion protein of the invention mayhave the ability to stimulate chondrocyte growth, therefore, they may beemployed to enhance bone and periodontal regeneration and aid in tissuetransplants or bone grafts.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may be also beemployed to prevent skin aging due to sunburn by stimulatingkeratinocyte growth.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be employedfor preventing hair loss, since FGF family members activate hair-formingcells and promotes melanocyte growth. Along the same lines, an albuminfusion protein of the invention and/or polynucleotide encoding analbumin fusion protein of the invention may be employed to stimulategrowth and differentiation of hematopoietic cells and bone marrow cellswhen used in combination with other cytokines.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be employedto maintain organs before transplantation or for supporting cell cultureof primary tissues. An albumin fusion protein of the invention and/orpolynucleotide encoding an albumin fusion protein of the invention mayalso be employed for inducing tissue of mesodermal origin todifferentiate in early embryos.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also increase ordecrease the differentiation or proliferation of embryonic stem cells,besides, as discussed above, hematopoietic lineage.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be used tomodulate mammalian characteristics, such as body height, weight, haircolor, eye color, skin, percentage of adipose tissue, pigmentation,size, and shape (e.g., cosmetic surgery). Similarly, an albumin fusionprotein of the invention and/or polynucleotide encoding an albuminfusion protein of the invention may be used to modulate mammalianmetabolism affecting catabolism, anabolism, processing, utilization, andstorage of energy.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may be used tochange a mammal's mental state or physical state by influencingbiorhythms, caricadic rhythms, depression (including depressivedisorders), tendency for violence, tolerance for pain, reproductivecapabilities (preferably by Activin or Inhibin-like activity), hormonalor endocrine levels, appetite, libido, memory, stress, or othercognitive qualities.

An albumin fusion protein of the invention and/or polynucleotideencoding an albumin fusion protein of the invention may also be used asa food additive or preservative, such as to increase or decrease storagecapabilities, fat content, lipid, protein, carbohydrate, vitamins,minerals, cofactors or other nutritional components.

The above-recited applications have uses in a wide variety of hosts.Such hosts include, but are not limited to, human, murine, rabbit, goat,guinea pig, camel, horse, mouse, rat, hamster, pig, micro-pig, chicken,goat, cow, sheep, dog, cat, non-human primate, and human. In specificembodiments, the host is a mouse, rabbit, goat, guinea pig, chicken,rat, hamster, pig, sheep, dog or cat. In preferred embodiments, the hostis a mammal. In most preferred embodiments, the host is a human.

Having generally described the invention, the same will be more readilyunderstood by reference to the following examples, which are provided byway of illustration and are not intended as limiting.

Without further description, it is believed that one of ordinary skillin the art can, using the preceding description and the followingillustrative examples, make and utilize the alterations detected in thepresent invention and practice the claimed methods. The followingworking examples therefore, specifically point out preferred embodimentsof the present invention, and are not to be construed as limiting in anyway the remainder of the disclosure.

EXAMPLES Example 1 Generation of pScNHSA and pScCHSA

The vectors pScNHSA (ATCC Deposit No. PTA-3279) and pScCHSA (ATCCDeposit No. PTA-3276) are derivatives of pPPC0005 (ATCC Deposit No.PTA-3278) and are used as cloning vectors into which polynucleotidesencoding a therapeutic protein or fragment or variant thereof isinserted adjacent to and in translation frame with polynucleotidesencoding human serum albumin “HSA”. pScCHSA may be used for generatingTherapeutic protein-HSA fusions, while pScNHSA may be used to generateHSA-Therapeutic protein fusions.

Generation of pScCHSA: Albumin Fusion with the Albumin Moiety C-Terminalto the Therapeutic Portion.

A vector to facilitate cloning DNA encoding a Therapeutic proteinN-terminal to DNA encoding the mature albumin protein was made byaltering the nucleic acid sequence that encodes the chimeric HSA signalpeptide in pPPC0005 to include the Xho I and Cla I restriction sites.

First, the Xho I and Cla I sites inherent to pPPC0005 (located 3′ of theADH1 terminator sequence) were eliminated by digesting pPPC0005 with XhoI and Cla I, filling in the sticky ends with T4 DNA polymerase, andreligating the blunt ends to create pPPC0006.

Second, the Xho I and Cla I restriction sites were engineered into thenucleic acid sequence that encodes the signal peptide of HSA (a chimeraof the HSA leader and a kex2 site from mating factor alpha, “MAF”) inpPPC0006 using two rounds of PCR. In the first round of PCR,amplification with primers shown as SEQ ID NO:1039 and SEQ ID NO:1040was performed. The primer whose sequence is shown as SEQ ID NO:1039comprises a nucleic acid sequence that encodes part of the signalpeptide sequence of HSA, a kex2 site from the mating factor alpha leadersequence, and part of the amino-terminus of the mature form of HSA. Fourpoint mutations were introduced in the sequence, creating the Xho I andCla I sites found at the junction of the chimeric signal peptide and themature form of HSA. These four mutations are underlined in the sequenceshown below. In pPPC0005 the nucleotides at these four positions from 5′to 3′ are T, G, T, and G.5′-GCCTCGAGAAAAGAGATGCACACAAGAGTGAGGTTGCTCATCGATTTAAAGAT TTGGG-3′ (SEQID NO:1039) and5′-AATCGATGAGCAACCTCACTCTTGTGTGCATCTCTTTTCTCGAGGCTCCTGGAA

TAAGC-3′ (SEQ ID NO:1040). A second round of PCR was then performed withan upstream flanking primer, 5′-TACAAACTTAAGAGTCCAATTAGC-3′ (SEQ IDNO:1041) and a downstream flanking primer5′-CACTTCTCTAGAGTGGTTTCATATGTCTT-3′ (SEQ ID NO:1042). The resulting PCRproduct was then purified and digested with Afl II and Xba I and ligatedinto the same sites in pPPC0006 creating pScCHSA. The resulting plasmidhas Xho I and Cla I sites engineered into the signal sequence. Thepresence of the Xho I site creates a single amino acid change in the endof the signal sequence from LDKR to LEKR. The D to E change will not bepresent in the final albumin fusion protein expression plasmid when anucleic acid sequence comprising a polynucleotide encoding theTherapeutic portion of the albumin fusion protein with a 5′ Sal I site(which is compatible with the Xho I site) and a 3′ Cla I site is ligatedinto the Xho I and Cla I sites of pScCHSA. Ligation of Sal I to Xho Irestores the original amino acid sequence of the signal peptidesequence. DNA encoding the Therapeutic portion of the albumin fusionprotein may be inserted after the Kex2 site (Kex2 cleaves after thedibasic amino acid sequence KR at the end of the signal peptide) andprior to the Cla I site.

Generation of pScNHSA: Albumin Fusion with the Albumin Moiety N-Terminalto the Therapeutic Portion.

A vector to facilitate cloning DNA encoding a Therapeutic proteinportion C-terminal to DNA encoding the mature albumin protein, was madeby adding three, eight-base-pair restriction sites to pScCHSA. The AscI, Fse I, and Pme I restriction sites were added in between the Bsu36 Iand Hind III sites at the end of the nucleic acid sequence encoding themature HSA protein. This was accomplished through the use of twocomplementary synthetic primers containing the Asc I, Fse I, and Pme Irestriction sites underlined (SEQ ID NO:1043 and SEQ ID NO:1044).

(SEQ ID NO: 1043) 5′-AAGCTGCCTTAGGCTTATAATAAGGCGCGCCGGCCGGCCGTTTAAACTAAGCTTAATTCT-3′ and (SEQ ID NO: 1044)5-AGAATTAAGCTTAGTTTAAACGGCCGGCCGGCGCGCCTTATTATAAG CCTAAGGCAGCTT-3′.These primers were annealed and digested with Bsu36 I and Hind III andligated into the same sites in pScCHSA creating pScNHSA.

Example 2 General Construct Generation for Yeast Transformation

The vectors pScNHSA and pScCHSA may be used as cloning vectors intowhich polynucleotides encoding a therapeutic protein or fragment orvariant thereof is inserted adjacent to polynucleotides encoding maturehuman serum albumin “HSA”. pScCHSA is used for generating Therapeuticprotein-HSA fusions, while pScNHSA may be used to generateHSA-Therapeutic protein fusions.

Generation of Albumin Fusion Constructs Comprising HSA-TherapeuticProtein Fusion Products.

DNA encoding a Therapeutic protein (e.g., sequences shown in SEQ ID NO:Xor known in the art) may be PCR amplified using the primers whichfacilitate the generation of a fusion construct (e.g., by addingrestriction sites, encoding seamless fusions, encoding linker sequences,etc.) For example, one skilled in the art could design a 5′ primer thatadds polynucleotides encoding the last four amino acids of the matureform of HSA (and containing the Bsu36I site) onto the 5′ end of DNAencoding a Therapeutic protein; and a 3′ primer that adds a STOP codonand appropriate cloning sites onto the 3′ end of the Therapeutic proteincoding sequence. For instance, the forward primer used to amplify DNAencoding a Therapeutic protein might have the sequence,5′-aagctGCCTTAGGCTTA(N)₁₅-3′ (SEQ ID NO:1045) where the underlinedsequence is a Bsu36I site, the upper case nucleotides encode the lastfour amino acids of the mature HSA protein (ALGL), and (N)₁₅ isidentical to the first 15 nucleotides encoding the Therapeutic proteinof interest. Similarly, the reverse primer used to amplify DNA encodinga Therapeutic protein might have the sequence,

(SEQ ID NO: 1046)

where the italicized sequence is a Pme I site, the double underlinedsequence is an Fse I site, the singly underlined sequence is an Asc Isite, the boxed nucleotides are the reverse complement of two tandemstop codons, and (N)₁₅ is identical to the reverse complement of thelast 15 nucleotides encoding the Therapeutic protein of interest. Oncethe PCR product is amplified it may be cut with Bsu36I and one of (AscI, Fse I, or Pme I) and ligated into pScNHSA.

The presence of the Xho I site in the HSA chimeric leader sequencecreates a single amino acid change in the end of the chimeric signalsequence, i.e. the HSA-kex2 signal sequence, from LDKR (SEQ ID NO:2139)to LEKR (SEQ ID NO:2140).

Generation of Albumin Fusion Constructs Comprising Gene-HSA FusionProducts.

Similar to the method described above, DNA encoding a Therapeuticprotein may be PCR amplified using the following primers: A 5′ primerthat adds polynucleotides containing a SalI site and encoding the lastthree amino acids of the HSA leader sequence, DKR, onto the 5′ end ofDNA encoding a Therapeutic protein; and a 3′ primer that addspolynucleotides encoding the first few amino acids of the mature HSAcontaining a Cla I site onto the 3′ end of DNA encoding a Therapeuticprotein. For instance, the forward primer used to amplify the DNAencoding a Therapeutic protein might have the sequence,5′-aggagcgtcGACAAAAGA(N)₁₅-3′ (SEQ ID NO:1047) where the underlinedsequence is a Sal I site, the upper case nucleotides encode the lastthree amino acids of the HSA leader sequence (DKR), and (N),₅ isidentical to the first 15 nucleotides encoding the Therapeutic proteinof interest. Similarly, the reverse primer used to amplify the DNAencoding a Therapeutic protein might have the sequence,

(SEQ ID NO: 1048) 5′-CTTTAAATCG ATGAGCAACCTCACTCTTGTGTGCATC(N)₁₅-3′where the italicized sequence is a Cla I site, the underlinednucleotides are the reverse complement of the DNA encoding the first 9amino acids of the mature form of HSA (DAHKSEVAH, SEQ ID NO:1106), and(N)′₅ is identical to the reverse complement of the last 15 nucleotidesencoding the Therapeutic protein of interest. Once the PCR product isamplified it may be cut with Sal I and Cla I and ligated into pScCHSAdigested with Xho I and Cla I. A different signal or leader sequence maybe desired, for example, invertase “INV” (Swiss-Prot Accession P00724),mating factor alpha “MAF” (Genbank Accession AAA18405), MPIF (GeneseqAAF82936), Fibulin B (Swiss-Prot Accession P23142), Clusterin(Swiss-Prot Accession P10909), Insulin-Like Growth Factor-BindingProtein 4 (Swiss-Prot Accession P22692), and permutations of the HSAleader sequence can be subcloned into the appropriate vector by means ofstandard methods known in the art.Generation of Albumin Fusion Construct Compatible for Expression inYeast S. cerevisiae.

The Not I fragment containing the DNA encoding either an N-terminal orC-terminal albumin fusion protein generated from pScNHSA or pScCHSA maythen be cloned into the Not I site of pSAC35 which has a LEU2 selectablemarker. The resulting vector is then used in transformation of a yeastS. cerevisiae expression system.

Example 3 General Expression in Yeast S. cerevisiae

An expression vector compatible with yeast expression can be transformedinto yeast S. cerevisiae by lithium acetate transformation,electroporation, or other methods known in the art and or as describedin part in Sambrook, Fritsch, and Maniatis. 1989. “Molecular Cloning: ALaboratory Manual, 2^(nd) edition”, volumes 1-3, and in Ausubel et al.2000. Massachusetts General Hospital and Harvard Medical School “CurrentProtocols in Molecular Biology”, volumes 1-4. The expression vectors areintroduced into S. cerevisiae strains DXY1, D88, or BXP10 bytransformation, individual transformants can be grown, for example, for3 days at 30° C. in 10 mL YEPD (1% w/v yeast extract, 2% w/v, peptone,2% w/v, dextrose), and cells can be collected at stationary phase after60 hours of growth. Supernatants are collected by clarifying cells at3000 g for 10 minutes.

pSAC35 (Sleep et al., 1990, Biotechnology 8:42 and see FIG. 3)comprises, in addition to the LEU2 selectable marker, the entire yeast 2μm plasmid to provide replication functions, the PRB1 promoter, and theADH1 termination signal.

Example 4 General Purification of an Albumin Fusion Protein Expressedfrom an Albumin Fusion in Yeast S. cerevisiae

In preferred embodiments, albumin fusion proteins of the inventioncomprise the mature form of HSA fused to either the N- or C-terminus ofthe mature form of a therapeutic protein or portions thereof (e.g., themature form of a therapeutic protein listed in Table 1, or the matureform of a therapeutic protein shown in Table 2 as SEQ ID NO:Z). In oneembodiment of the invention, albumin fusion proteins of the inventionfurther comprise a signal sequence which directs the nascent fusionpolypeptide in the secretory pathways of the host used for expression.In a preferred embodiment, the signal peptide encoded by the signalsequence is removed, and the mature albumin fusion protein is secreteddirectly into the culture medium. Albumin fusion proteins of theinvention preferably comprise heterologous signal sequences (e.g., thenon-native signal sequence of a particular therapeutic protein)including, but not limited to, MAF, INV, Ig, Fibulin B, Clusterin,Insulin-Like Growth Factor Binding Protein 4, variant HSA leadersequences including, but not limited to, a chimeric HSA/MAF leadersequence, or other heterologous signal sequences known in the art.Especially preferred as those signal sequence listed in Table 2 and/orthe signal sequence listed in the “Expression of Fusion Proteins” and/or“Additional Methods of Recombinant and Synthetic Production of AlbuminFusion Proteins” section of the specification, above. In preferredembodiments, the fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Albumin fusion proteins expressed in yeast as described above can bepurified on a small-scale over a Dyax peptide affinity column asfollows. Supernatants from yeast expressing an albumin fusion protein isdiafiltrated against 3 mM phosphate buffer pH 6.2, 20 mM NaCl and 0.01%Tween 20 to reduce the volume and to remove the pigments. The solutionis then filtered through a 0.22 μm device. The filtrate is loaded onto aDyax peptide affinity column. The column is eluted with 100 mM Tris/HCl,pH 8.2 buffer. The peak fractions containing protein are collected andanalyzed on SDS-PAGE after concentrating 5-fold.

For large scale purification, the following method can be utilized. Thesupernatant in excess of 2 L is diafiltered and concentrated to 500 mLin 20 mM Tris/HCl pH 8.0. The concentrated protein solution is loadedonto a pre-equilibrated 50 mL DEAE-Sepharose Fast Flow column, thecolumn is washed, and the protein is eluted with a linear gradient ofNaCl from 0 to 0.4 M NaCl in 20 mM Tris/HCl, pH 8.0. Those fractionscontaining the protein are pooled, adjusted to pH 6.8 with 0.5 M sodiumphosphate (NaH₂PO₄). A final concentration of 0.9 M (NH₄)₂SO₄ is addedto the protein solution and the whole solution is loaded onto apre-equilibrated 50 mL Butyl650S column. The protein is eluted with alinear gradient of ammonium sulfate (0.9 to 0 M (NH₄)₂SO₄). Thosefractions with the albumin fusion are again pooled, diafiltered against10 mM Na₂HPO₄/citric acid buffer pH 5.75, and loaded onto a 50 mLpre-equilibrated SP-Sepharose Fast Flow column. The protein is elutedwith a NaCl linear gradient from 0 to 0.5 M. The fractions containingthe protein of interest are combined, the buffer is changed to 10 mMNa₂HPO₄/citric acid pH 6.25 with an Amicon concentrator, theconductivity is <2.5 mS/cm. This protein solution is loaded onto a 15 mLpre-equilibrated Q-Sepharose high performance column, the column iswashed, and the protein is eluted with a NaCl linear gradient from 0 to0.15 M NaCl. The purified protein can then be formulated into a specificbuffer composition by buffer exchange.

Example 5 General Construct Generation for Mammalian Cell TransfectionGeneration of Albumin Fusion Construct Compatible for Expression inMammalian Cell-Lines.

Albumin fusion constructs can be generated in expression vectors for usein mammalian cell culture systems. DNA encoding a therapeutic proteincan be cloned N-terminus or C-terminus to HSA in a mammalian expressionvector by standard methods known in the art (e.g., PCR amplification,restriction digestion, and ligation). Once the expression vector hasbeen constructed, transfection into a mammalian expression system canproceed. Suitable vectors are known in the art including, but notlimited to, for example, the pC4 vector, and/or vectors available fromLonza Biologics, Inc. (Portsmouth, N.H.).

The DNA encoding human serum albumin has been cloned into the pC4 vectorwhich is suitable for mammalian culture systems, creating plasmidpC4:HSA (ATCC Deposit # PTA-3277). This vector has a DiHydroFolateReductase, “DHFR”, gene that will allow for selection in the presence ofmethotrexate.

The pC4:HSA vector is suitable for expression of albumin fusion proteinsin CHO cells. For expression, in other mammalian cell culture systems,it may be desirable to subclone a fragment comprising, or alternativelyconsisting of, DNA which encodes for an albumin fusion protein into analternative expression vector. For example, a fragment comprising, oralternatively consisting, of DNA which encodes for a mature albuminfusion protein may be subcloned into another expression vectorincluding, but not limited to, any of the mammalian expression vectorsdescribed herein.

In a preferred embodiment, DNA encoding an albumin fusion construct issubcloned into vectors provided by Lonza Biologics, Inc. (Portsmouth,N.H.) by procedures known in the art for expression in NS0 cells.

Generation of Albumin Fusion Constructs Comprising HSA-TherapeuticProtein Fusion Products.

Using pC4:HSA (ATCC Deposit # PTA-3277), albumin fusion constructs canbe generated in which the Therapeutic protein portion is C terminal tothe mature albumin sequence. For example, one can clone DNA encoding aTherapeutic protein of fragment or variant thereof between the Bsu 36Iand Asc I restriction sites of the vector. When cloning into the Bsu 36Iand Asc I, the same primer design used to clone into the yeast vectorsystem (SEQ ID NO:1045 and 1046) may be employed (see Example 2).

Generation of Albumin Fusion Constructs Comprising Gene-HSA FusionProducts.

Using pC4:HSA (ATCC Deposit # PTA-3277), albumin fusion constructs canbe generated in which a Therapeutic protein portion is cloned N terminalto the mature albumin sequence. For example, one can clone DNA encodinga Therapeutic protein that has its own signal sequence between the BamHI (or Hind III) and Cla I sites of pC4:HSA. When cloning into eitherthe Bam HI or Hind III site, it is preferable to include a Kozaksequence (CCGCCACCATG, SEQ ID NO:1107) prior to the translational startcodon of the DNA encoding the Therapeutic protein. If a Therapeuticprotein does not have a signal sequence, DNA encoding that Therapeuticprotein may be cloned in between the Xho I and Cla I sites of pC4:HSA.When using the Xho I site, the following 5′ (SEQ ID NO:1052) and 3′ (SEQID NO:1053) exemplary PCR primers may be used:

(SEQ ID NO: 1052) 5′-CCGCCGCTCGAGGGGTGTGTTTCGTCGA(N)₁₈-3′(SEQ ID NO: 1053) 5′-AGTCCCATCGATGAGCAACCTCACTCTTGTGTGCATC(N)₁₈-3′

In the 5′ primer (SEQ ID NO:1052), the underlined sequence is a Xho Isite; and the Xho I site and the DNA following the Xho I site code forthe last seven amino acids of the leader sequence of natural human serumalbumin. In SEQ ID NO:1052, “(N)₁₈” is DNA identical to the first 18nucleotides encoding the Therapeutic protein of interest. In the 3′primer (SEQ ID NO:1053), the underlined sequence is a Cla I site; andthe Cla I site and the DNA following it are the reverse complement ofthe DNA encoding the first 10 amino acids of the mature HSA protein (SEQID NO:1038). In SEQ ID NO:1053 “(N)₁₈” is the reverse complement of DNAencoding the last 18 nucleotides encoding the Therapeutic protein ofinterest. Using these two primers, one may PCR amplify the Therapeuticprotein of interest, purify the PCR product, digest it with Xho I andCla I restriction enzymes and clone it into the Xho I and Cla I sites inthe pC4:HSA vector.

If an alternative leader sequence is desired, the native albumin leadersequence can be replaced with the chimeric albumin leader, i.e., theHSA-kex2 signal peptide, or an alternative leader by standard methodsknown in the art. (For example, one skilled in the art could routinelyPCR amplify an alternate leader and subclone the PCR product into analbumin fusion construct in place of the albumin leader whilemaintaining the reading frame)

Example 6 General Expression in Mammalian Cell-Lines

An albumin fusion construct generated in an expression vector compatiblewith expression in mammalian cell-lines can be transfected intoappropriate cell-lines by calcium phosphate precipitation,lipofectamine, electroporation, or other transfection methods known inthe art and/or as described in Sambrook, Fritsch, and Maniatis. 1989.“Molecular Cloning: A Laboratory Manual, 2^(nd) edition” and in Ausubelet al. 2000. Massachusetts General Hospital and Harvard Medical School“Current Protocols in Molecular Biology”, volumes 1-4. The transfectedcells are then selected for by the presence of a selecting agentdetermined by the selectable marker in the expression vector.

The pC4 expression vector (ATCC Accession No. 209646) is a derivative ofthe plasmid pSV2-DHFR (ATCC Accession No. 37146). pC4 contains thestrong promoter Long Terminal Repeats “LTR” of the Rous Sarcoma Virus(Cullen et al., March 1985, Molecular and Cellular Biology, 438-447) anda fragment of the CytoMegaloVirus “CMV”-enhancer (Boshart et al., 1985,Cell 41: 521-530). The vector also contains the 3′ intron, thepolyadenylation and termination signal of the rat preproinsulin gene,and the mouse DHFR gene under control of the SV40 early promoter.Chinese hamster ovary “CHO” cells or other cell-lines lacking an activeDHFR gene are used for transfection. Transfection of an albumin fusionconstruct in pC4 into CHO cells by methods known in the art will allowfor the expression of the albumin fusion protein in CHO cells, followedby leader sequence cleavage, and secretion into the supernatant. Thealbumin fusion protein is then further purified from the supernatant.

The pEE12.1 expression vector is provided by Lonza Biologics, Inc.(Portsmouth, N.H.) and is a derivative of pEE6 (Stephens and Cockett,1989, Nucl. Acids Res. 17: 7110). This vector comprises a promoter,enhancer and complete 5′-untranslated region of the Major ImmediateEarly gene of the human CytoMegaloVirus, “hCMV-MIE” (InternationalPublication # WO89/01036), upstream of a sequence of interest, and aGlutamine Synthetase gene (Murphy et al., 1991, Biochem J. 227: 277-279;Bebbington et al., 1992, Bio/Technology 10:169-175; U.S. Pat. No.5,122,464) for purposes of selection of transfected cells in selectivemethionine sulphoximine containing medium. Transfection of albuminfusion constructs made in pEE12.1 into NS0 cells (InternationalPublication # WO86/05807) by methods known in the art will allow for theexpression of the albumin fusion protein in NS0 cells, followed byleader sequence cleavage, and secretion into the supernatant. Thealbumin fusion protein is then further purified from the supernatantusing techniques described herein or otherwise known in the art.

Expression of an albumin fusion protein may be analyzed, for example, bySDS-PAGE and Western blot, reversed phase HPLC analysis, or othermethods known in the art.

Stable CHO and NS0 cell-lines transfected with albumin fusion constructsare generated by methods known in the art (e.g., lipofectaminetransfection) and selected, for example, with 100 nM methotrexate forvectors having the DiHydroFolate Reductase ‘DHFR’ gene as a selectablemarker or through growth in the absence of glutamine. Expression levelscan be examined for example, by immunoblotting, primarily, with ananti-HSA serum as the primary antibody, or, secondarily, with serumcontaining antibodies directed to the Therapeutic protein portion of agiven albumin fusion protein as the primary antibody.

Expression levels are examined by immunoblot detection with anti-HSAserum as the primary antibody. The specific productivity rates aredetermined via ELISA in which the capture antibody can be a monoclonalantibody towards the therapeutic protein portion of the albumin fusionand the detecting antibody can be the monoclonal anti-HSA-biotinylatedantibody (or vice versa), followed by horseradishperoxidase/streptavidin binding and analysis according to themanufacturer's protocol.

Example 7 General Purification of an Albumin Fusion Protein Expressedfrom an Albumin Fusion Construct in Mammalian Cell-Lines

In preferred embodiments, albumin fusion proteins of the inventioncomprise the mature form of HSA fused to either the N- or C-terminus ofthe mature form of a therapeutic protein or portions thereof (e.g., themature form of a therapeutic protein listed in Table 1, or the matureform of a therapeutic protein shown in Table 2 as SEQ ID NO:Z). In oneembodiment of the invention, albumin fusion proteins of the inventionfurther comprise a signal sequence which directs the nascent fusionpolypeptide in the secretory pathways of the host used for expression.In a preferred embodiment, the signal peptide encoded by the signalsequence is removed, and the mature albumin fusion protein is secreteddirectly into the culture medium. Albumin fusion proteins of theinvention preferably comprise heterologous signal sequences (e.g., thenon-native signal sequence of a particular therapeutic protein)including, but not limited to, MAF, INV, Ig, Fibulin B, Clusterin,Insulin-Like Growth Factor Binding Protein 4, variant HSA leadersequences including, but not limited to, a chimeric HSA/MAF leadersequence, or other heterologous signal sequences known in the art.Especially preferred as those signal sequence listed in Table 2 and/orthe signal sequence listed in the “Expression of Fusion Proteins” and/or“Additional Methods of Recombinant and Synthetic Production of AlbuminFusion Proteins” section of the specification, above. In preferredembodiments, the fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Albumin fusion proteins from mammalian cell-line supernatants arepurified according to different protocols depending on the expressionsystem used.

Purification from CHO and 293T Cell-Lines.

Purification of an albumin fusion protein from CHO cell supernatant orfrom transiently transfected 293T cell supernatant may involve initialcapture with an anionic HQ resin using a sodium phosphate buffer and aphosphate gradient elution, followed by affinity chromatography on aBlue Sepharose FF column using a salt gradient elution. Blue SepharoseFF removes the main BSA/fetuin contaminants. Further purification overthe Poros PI 50 resin with a phosphate gradient may remove and lowerendotoxin contamination as well as concentrate the albumin fusionprotein.

Purification from NS0 Cell-Line.

Purification of an albumin-fusion protein from NS0 cell supernatant mayinvolve Q-Sepharose anion exchange chromatography, followed bySP-sepharose purification with a step elution, followed by Phenyl-650Mpurification with a step elution, and, ultimately, diafiltration.

The purified protein may then be formulated by buffer exchange.

Example 8 Construct ID 1966, EPO-HSA, Generation

Construct ID 1966, pC4.EPO:M1-D192.HSA, encodes for an EPO-HSA fusionprotein which comprises the EPO native leader sequence as well as themature EPO protein with the exception of the final Arg residue, i.e.,M1-D192, fused to the amino-terminus of the mature form of HSA clonedinto the mammalian expression vector pC4.

Cloning of EPO cDNA for Construct 1966

The DNA encoding EPO was amplified with primers EPO1 and EPO2, describedbelow, cut with Bam HI/Cla I, and ligated into Bam HI/Cla I cut pC4:HSA.Construct ID #1966 encodes an albumin fusion protein containing theleader sequence and the mature form of EPO, followed by the mature HSAprotein (see SEQ ID NO:297 for construct 1966 in table 2).

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the full length EPO including the natural leadersequence (SEQ ID NO:81, table 2), EPO1 and EPO2, were synthesized.

EPO1: (SEQ ID NO: 1122) 5′-GACTGGAT CCGCCACCATGGGGGTGCACGAATGTCCTGCCTGGCTGTGGCTTCTCCTGTCCCTGCTGTCGCTCCCTCTGGGCCTCCCAGTCCTGGGCGCCCCACCACGCCTCATCTGTGAC-3′ EPO2: (SEQ ID NO: 804)5′-AGTCCCATCGATGAGCAACCTCACTCTTGTGTGCATCGTCCCCTGTC CTGCAGGCCTCC-3′

EPO1 incorporates a Bam HI cloning site (shown in italics) and attachesa kozak sequence (shown double underlined) prior to the DNA encoding thefirst 35 amino acids of the ORF of the full-length EPO. In EPO2, theunderlined sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein (SEQ ID NO:1038). In EPO2, thebolded sequence is the reverse complement of the last 22 nucleotidesencoding amino acid residues Glu-186 to Asp-192 of the full-length formof EPO, with the exception of the final Arg residue. Using these twoprimers, the full-length EPO protein, with the exception of the finalArg residue, was PCR amplified. Annealing and extension temperatures andtimes must be empirically determined for each specific primer pair andtemplate.

The PCR product was purified (for example, using Wizard PCR Preps DNAPurification System (Promega Corp)) and then digested with Bam HI andCla I. After further purification of the Bam HI-Cla I fragment by gelelectrophoresis, the product was cloned into Bam HI/Cla I digestedpC4:HSA to produce construct ID #1966.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedEPO sequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1966. Expression in Either293T or CHO Cells.

Construct 1966 was transfected into either 293T cells or CHO cells bymethods known in the art (e.g., lipofectamine transfection) and selectedwith 100 nM methotrexate (see Example 6). Expression levels wereexamined by immunoblot detection with anti-HSA serum as the primaryantibody, and the specific productivity rates were determined via ELISAusing a monoclonal anti-human EPO antibody (Research Diagnostics, Inc.)for capture and a Biotrend monoclonal anti-HSA-biotinylated antibody fordetection, followed by horseradish peroxidase/streptavidin binding andanalysis.

Purification from 293T Cell Supernatant.

The 293T cell supernatant containing the secreted EPO-HSA fusion proteinexpressed from construct ID #1966 in 293T cells was purified asdescribed in Example 7. Specifically, initial capture was performed withan anionic HQ-50 resin at pH 7.2 using a step elution, followed by Bluesepharose FF chromatography again employing a step elution at pH 7.2.The pooled fractions were passed over the HQ-50 resin again using a stepelution. The eluted sample was then loaded onto the Phenyl-650M columnand eluted with a gradient elution at pH 7.2. The eluted sample waspassed over the HQ-50 resin for a third time. The fractions of interestwere diafiltrated into 50 mM Na₂HPO₄+200 mM NaCl pH 7.2. N-terminalsequencing generated the amino-terminus sequence (i.e., APPRLI) of themature form of EPO. A protein of approximate MW of 90 kDa was obtained.A final yield of 0.42 mg protein per litre of 293T cell supernatant wasobtained.

Purification from CHO Cell Supernatant.

The cell supernatant containing the EPO-albumin fusion protein expressedfrom construct ID #1966 in CHO cells was purified as described inExample 7. Specifically, initial capture of a concentrated 1.4 L samplewas performed with an anionic Poros HQ 50 resin using a sodium phosphatebuffer and a phosphate gradient elution (0-100 mM sodium phosphate, pH7.2). Prior to loading the column, the sample was diluted with 3 mMphosphate until the conductivity was lower than 5.0 mS, as was the casefor further column chromatography purifications. The HQ resin wasequilibrated with 10 mM sodium phosphate, pH 7.2 prior to sampleloading. EPO-HSA eluted at 20 mS, or 50 mM sodium phosphate. The secondpurification step involved affinity chromatography. The combinedfractions from the previous HQ resin elution, adjusted for aconductivity <5 mS using 3 mM phosphate pH 7.2 buffer, were loaded ontoa Blue Sepharose FF column equilibrated with 125 mM NaCl, 15 mM sodiumphosphate, pH 7.2. A salt gradient of 0-3 M NaCl eluted EPO-HSA between0.5 M and 1.0 M NaCl. Blue Sepharose FF removes the main BSA/fetuincontaminants. The conductivity of the desired fractions was againadjusted for, and the pooled fractions were loaded onto a third columncontaining Poros PI 50 resin which removes and lowers endotoxincontamination as well as concentrates the EPO-HSA protein. The resin wasequilibrated with 25 mM NaCl, 10 mM sodium phosphate, pH 7.2. EPO-HSAwas eluted with a 10 mM-100 mM phosphate gradient. The final buffercomposition was 100 mM NaCl, 20 mM Na₂HPO₄, pH 7.2. An approximateprotein MW of 87.7 kDa was obtained. A final yield of 8.9 mg protein perliter of supernatant was obtained. N-Terminal sequencing generated thesequence APPRL which corresponds to the amino-terminus of the matureform of EPO.

In Vitro TF-1 Cell Proliferation Assay. Method

The biological activity of an EPO albumin fusion protein can be measuredin an in vitro TF-1 cell proliferation assay. The TF-1 cell-line wasestablished by Kitamura et al. (Kitamura, T. et al., 1989, J. Cell.Physiol., 140: 323-334). The TF-1 cells were derived from a heparinizedbone marrow aspiration sample from a 35 year old Japanese male withsevere pancytopenia. The TF-1 cell-line provides a good system forinvestigating the proliferation and differentiation of myeloidprogenitor cells as a result of its responsiveness to multiplecytokines.

TF-1 cell proliferation assay (Kitamura, T. et al., 1989, J. Cell.Physiol., 140: 323-334): Human TF-1 cells (ATCC # CRL-2003) are expandedin RPMI 1640 media containing 10% FBS, 1× pen-strep, 1× L-glutamine, and2 ng/mL human GM-CSF to a maximum density of 1×10⁶ cells/mL. Cells arepassaged every 2-3 days by diluting 1:10 or 1:20 in fresh medium. On theday of the assay initiation, cells are washed in a 50 mL volume of RPMI1640/10% FBS three times to remove GM-CSF and are resuspended at 1×10⁵cells/mL in RPMI 1640/10% FBS. Cells are plated at 10,000 cells/well inflat-bottom TC-treated 96-well plates. Three-fold serial dilutions ofcontrol protein are made in RPMI 1640/10% FBS in a range of 10 U/mL to0.001 U/mL (final concentration) and three-fold serial dilutions of analbumin fusion protein are made in RPMI 1640/10% FBS in a range of 100ng/mL to 0.01 ng/mL (final concentration) where 1 U=10 ng protein; 0.1mL of each dilution is added to triplicate wells containing cells for afinal volume of 0.2 mL in each well. Cell proliferation response to thecontrol protein and the albumin fusion protein is determined bymeasuring incorporation of ³H-thymidine (0.5 uCi/well). The assay iscarried out at incubation times of 24, 48, or 72 hours prior to and for4-24 hours after the addition of ³H-thymidine. Since only a portion ofthe molar weight of an albumin fusion protein is actually a therapeuticprotein molecule (i.e., the therapeutic protein portion of the fusion),in some cases dilutions may also be adjusted for the molar ratio.

In Vitro TF-1 Cell Proliferation Assay for the Albumin Fusion ProteinEncoded by Construct 1966. Method

TF-1 cell proliferation assay: Human TF-1 cells (ATCC # CRL-2003) wereexpanded in RPMI 1640 media containing 10% FBS, 1× pen-strep, 1×L-glutamine, and 2 ng/mL human GM-CSF to a maximum density of 1×10⁶cells/mL. Cells were passaged every 2-3 days by diluting 1:10 or 1:20 infresh medium. On the day of the assay initiation, cells were washed in a50 mL volume of RPMI 1640/10% FBS three times to remove GM-CSF and wereresuspended at 1×10⁵ cells/mL in RPMI 1640/10% FBS. Cells were plated at10,000 cells/well in flat-bottom TC-treated 96-well plates. Three-foldserial dilutions of hrEPO (R&D Systems; Research Diagnostics Inc., RDI)were made in RPMI 1640/10% FBS in a range of 10 U/mL to 0.001 U/mL(final concentration) and three-fold serial dilutions of the EPO albuminfusion protein were made in RPMI 1640/10% FBS in a range of 100 ng/mL to0.01 ng/mL (final concentration) where 1 U=10 ng protein; 0.1 mL of eachdilution was added to triplicate wells containing cells for a finalvolume of 0.2 mL in each well. Cell proliferation response to hrEPO andEPO albumin protein was determined by measuring incorporation of³H-thymidine (0.5 μCi/well). The assay was carried out at incubationtimes of 24, 48, or 72 hours prior to and for 4-24 hours after theaddition of ³H-thymidine. Since only ⅓ of the molar weight of the EPOalbumin fusion protein is actually an EPO molecule, in some casesdilutions made were also to adjust for the molar ratio.

Results

Supernatants from 293T cells expressing construct 1966 or >90% purifiedEPO-HSA albumin fusion protein derived from CHO cells expressingconstruct 1966 were tested in the above assay for EPO activity. Onaverage, an EC50 of greater than 5 fold of that of rhEPO was established(see FIG. 4).

In Vivo Harlan Mouse Model for Measuring Hematocrit. Methods

This mouse model provides the means to measure the therapeutic activityof a protein in vivo by measuring its effect on the hematocrit.

An in vivo mouse model, i.e., 6-8 week old female DBA/2NHsd mice(Harlan), has been established to monitor the effect on hematocrit uponadministration of a control protein at 2 μs/kg and at otherconcentrations or an albumin fusion protein at 30 μs/kg and at otherconcentrations daily or every other day for 7 days either intravenously,intraperitoneally, or subcutaneously. Hematocrit is determined bysticking the tail vein with a needle, collecting the blood with aheparinized microcapillary tube, and then spinning the tubes throughoutthe experimental time-frame. Also, for certain experiments, the spleenis harvested and weighed. Other dosing schedules are known within theart and can readily be adapted for use in this assay.

The Activity of the Albumin Fusion Protein Encoded by Construct 1966 canbe Assayed Using an In Vivo Harlan Mouse Model for Measuring Hematocrit.Methods

An in vivo mouse model of 6-8 week old female DBA/2NHsd mice (Harlan)was used to monitor the extent of EPO activity upon administration ofrhEPO (Research Diagnostics, Inc., cat # RDI-PB11965) at doses of 0.5,1.5, 4.5, and 12 μs/kg on days 0, 2, 4 and 6 and upon administration ofthe purified EPO albumin fusion protein encoded by construct 1966 atconcentrations of 2, 6, 18, and 54 μs/kg on days 0, 2, 4, and 6subcutaneously, “SC”. Hematocrit was determined by sticking the tailvein with a needle on days 0 and 7, collecting the blood with aheparinized microcapillary tube, and then spinning the tubes throughoutthe experimental time-frame. The higher doses of the EPO albumin fusionprotein is a rough equimolar comparison with the control recombinanthuman EPO, “rhEPO” (Research Diagnostics, Inc., cat # RDI-PB 11965).

Results

There was a significant increase in hematocrit (see FIG. 5) from day 0to day 7 for animals treated with either recombinant human EPO or EPOalbumin fusion proteins. However, the EPO albumin fusion protein encodedby construct 1966 appeared to have a more drastic effect on hematocritlevels than the rhEPO control. Subcutaneous administration of 3doses/week of 52 μs/kg, or 1 dose/week of 156 μs/kg, of the EPO albuminfusion protein encoded by construct 1966 caused a greater than or equalto 40% change in hematocrit from day 0 to day 8 (see FIG. 6). The %change in hematocrit was either maintained close to 40% for the tripledose or subdued to ˜20% for the single dose on day 14 as opposed to adecline from close to 30% to <10% for a 3 dose subcutaneousadministration of 12 μs/kg of rhEPO in a week. The elevated hematocritappears to be maintained with the EPO albumin fusion protein encoded byconstruct 1966 over a period of a week after the last subcutaneousadministration in comparison with the hematocrit levels induced by therhEPO protein which declines back to more normal levels.

DBA mice injected intravenously with a 150 μs/kg dose of the EPO albuminfusion protein encoded by albumin fusion construct 1966 cleared this EPOalbumin fusion protein 7 times more slowly than rhEPO.

Example 9 Construct ID 1981, HSA-EPO, Generation

Construct ID 1981, pC4.HSA-EPO.A28-D192, comprises DNA encoding for anEPO albumin fusion protein which has the HSA full-length sequence,including the native HSA leader sequence, fused to the amino terminus ofthe mature form of EPO, with the exception of the final Arg residue,cloned into the mammalian expression vector pC4.

Cloning of EPO cDNA for Construct 1981

The DNA encoding EPO was amplified with primers EPO3 and EPO4, describedbelow, cut with Bsu 36I/Asc I, and ligated into Bsu 36I/Asc I cutpC4:HSA. Construct ID #1981 encodes an albumin fusion protein containingthe native leader sequence and mature form of HSA and the mature form ofEPO, Ala 28 to Asp 192 (Genbank Accession AAA52400).

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the mature form of EPO (see SEQ ID NO:X forconstruct 1981 in Table 2), EPO3 and EPO4, were synthesized:

EPO3: (SEQ ID NO: 805) 5′-AAGCTGCCTTAGGCTTAGCCCCACCACGCCTCATCTGTGACAG-3′EPO4: (SEQ ID NO: 806)5′-GCGCGGCGCGCCGAATTCCTATTAGTCCCCTGTCCTGCAGGCCTCCC CTGTG-3′

EPO3 incorporates a Bsu 36I cloning site (shown underlined) andnucleotides encoding the last four amino acid residues of the matureform of HSA, as well as 26 nucleotides, italicized, encoding the first 8amino acid residues of the mature form of EPO. In EPO4, the Asc I siteis underlined (SEQ ID NO:806) and the last 28 nucleotides, italicized,are the reverse complement of DNA encoding the last 9 amino acidresidues of EPO (for general construct cloning see Example 5), with theexception of the final Arg residue. The PCR amplimer generated usingthese primers was purified, digested with Bsu 36I and Asc I restrictionenzymes, and cloned into the Bsu 36I and Asc I sites of the pC4:HSAvector.

The PCR product was purified (for example, by using Wizard PCR Preps DNAPurification System (Promega Corp)) and then digested with Bsu36I andAscI. After further purification of the Bsu36I-AscI fragment by gelelectrophoresis, the product was cloned into Bsu36I/AscI digestedpC4:HSA to give construct ID #1981.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedHSA sequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1981. Expression in CHOCells.

Construct 1981 was transfected into CHO cells as described in Examples 6and 8. Expression levels and the specific productivity rates weredetermined as described in Example 8.

Purification from CHO Supernatant.

The cell supernatant containing the EPO albumin fusion protein expressedfrom construct ID #1981 in CHO cells was purified as described inExamples 7 and 8. N-terminal sequencing generated DAHKS, the sequence ofthe amino terminus of the mature form of HSA. For each litre ofsupernatant, 14 mg of protein was obtained. An approximate MW of 85.7kDa was obtained.

In Vitro TF-1 Cell Proliferation Assay for Construct 1981. Method

The in vitro TF-1 cell proliferation assay for the EPO albumin fusionprotein encoded by construct 1981 was carried out as previouslydescribed in Example 8 under subsection heading “In vitro TF-1 cellproliferation assay for construct 1966”.

Results

Supernatants from CHO cells expressing construct 1981 were >90% purifiedfor the HSA-EPO albumin fusion protein and were tested in the assay, asdescribed in Example 8. On average, an EC50 of greater than 5 fold ofthat of rhEPO was established (see FIGS. 4 and 7).

The Activity of Construct 1981 can be Assayed Using an In Vivo HarlanMouse Model for Measuring Hematocrit. Methods

The in vivo Harlan mouse model was used to assay for hematocrit levelsupon subcutaneous administration of either control rhEPO or EPO albuminfusion protein encoded by construct 1981. The assay was carried out aspreviously described in Example 8 under subsection heading “The activityof construct 1966 can be assayed using an in vivo Harlan mouse model formeasuring hematocrit”.

Results

There was a significant increase in hematocrit (see FIG. 5) from day 0to day 7 for animals treated with either rhEPO or EPO albumin fusionproteins. However, the EPO albumin fusion protein encoded by construct1981 appears to have a more drastic effect on hematocrit levels than therhEPO control.

DBA mice injected intravenously with a 150 μs/kg dose of EPO albuminfusion protein encoded by albumin fusion construct 1981 cleared this EPOalbumin fusion protein 7 times more slowly than rhEPO.

Example 10 Construct ID 1997, EPO-HSA, Generation

Construct ID 1997, pEE12.1:EPO M1-D192.HSA, comprises DNA encoding anEPO albumin fusion protein which has the full-length EPO protein(including the native leader sequence), i.e., M1-D192, with theexception of the final Arg residue, fused to the amino-terminus of themature form of HSA cloned into the mammalian expression vector pEE12.1.

Cloning of EPO cDNA for Construct 1997.

The DNA encoding EPO was amplified with primers EPO5 and EPO6, describedbelow, cut with Eco RI/Cla I, and ligated into Eco RI/Cla I cut pcDNA3(Invitrogen Corporation, 1600 Faraday Ave, Carlsbad, Calif. 92008).pcDNA3.EPO M1-D192.HSA was digested with Eco RI/Hind III to release theEPO M1-D192.HSA expression cassette fragment and cloned into Eco RI/HindIII digested pEE12.1. Construct ID #1997 encodes an albumin fusionprotein containing the leader sequence and the mature form of EPO,followed by the mature HSA protein (see SEQ ID NO:Y in Table 2 forconstruct 1997).

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding EPO (SEQ ID NO:X, Table 2 for construct 1997),EPO5 and EPO6, were synthesized.

EPO5: (SEQ ID NO: 775) 5′-GATCGAATT CGCCACCATGGGGGTGCACGAATGTCCTGCCTGGCTGTGGCTTCTCCTGTCCCTGCTGTCGCTCCCTCTGGGCCTCCCAGTCCTGGGCGCCCCACCACGCCTCATCTGTGAC-3′ EPO6: (SEQ ID NO: 776) 5′-CTTTAAATCGATGAGCAACCTCACTCTTGTGTGCATCGTCCCCTG TCCTGCAGGCCTCCC-3′EPO5 incorporates an Eco RI site (shown in italics) and a kozak sequence(shown underlined) prior to the DNA encoding the first 35 amino acids ofthe ORF of the full-length EPO. In EPO6, the italicized sequence is aCla I site, the underlined sequence is the reverse complement of the DNAencoding the first 9 amino acids of the mature form of HSA protein(DAHKSEVAH, SEQ ID NO:1106), and the sequence following the reversecomplement of HSA is the reverse complement of the last 23 nucleotidesencoding the last 7 amino acids of EPO not including the final Arg-193amino acid. Using these two primers, DNA encoding the full-length EPOprotein was PCR amplified as in Example 8.

The PCR product was purified and then digested with Eco RI and Cla I.After further purification of the Eco RI-Cla I fragment by gelelectrophoresis, the product was cloned into Eco RI/Cla I digestedpcDNA3. The Eco RI/Hind III fragment containing the expression cassettewas generated from pcDNA3.EPO.M1-D192.HSA and subcloned into the EcoRI/Hind III digested pEE12.1 to give construct ID #1997.

Further, analysis of the N-terminus of the albumin fusion protein byamino acid sequencing confirmed the presence of the expected EPOsequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1997. Expression in NS0Cells.

Construct 1997 was transfected into NS0 cells as described in Example 6.Expression levels and specific productivity rates were determined asdescribed in Example 8.

Purification from NS0 Cell Supernatant.

Purification of the EPO albumin fusion protein from 500 mL cellsupernatant from NSO cells transfected with construct 1997 involvesQ-Sepharose anion exchange chromatography at pH 7.4 using a NaClgradient from 0 to 1 M in 20 mM Tris-HCl, followed by Poros PI 50 anionexchange chromatography at pH 6.5 with a sodium citrate gradient from 5to 40 mM, and diafiltrating for 6 DV into 10 mM citrate, pH 6.5 and 140mM NaCl, the final buffer composition (see, Example 7). N-terminalsequencing yielded the sequence APPRLI which is the amino terminus ofthe mature form of EPO. The protein has an approximate MW of 87.7 kDa. Afinal yield of 52.2 mg protein per L of supernatant was obtained.

For larger scale purification, 50 L of NS0 cell supernatant can beconcentrated into ˜8 to 10 L. The concentrated sample can then be passedover the Q-Sepharose anion exchange column (10×19 cm, 1.5 L) at pH 7.5using a step elution consisting of 50 mM NaOAc, pH 6.0 and 150 mM NaCl.The eluted sample can then be virally inactivated with 0.75% Triton-X100 for 60 min at room temperature. SDR-Reverse Phase chromatography (10cm×10 cm, 0.8 L) can then be employed at pH 6.0 with 50 mM NaOAc and 150mM NaCl, or alternatively, the sample can be passed over an SP-sepharosecolumn at pH 4.8 using a step elution of 50 mM NaOAc, pH 6.0, and 150 mMNaCl. DV 50 filtration would follow to remove any viral content.Phenyl-650M chromatography (20 cm×12 cm, 3.8 L) at pH 6.0 using a stepelution consisting of 350 mM (NH₄)₂SO₄ and 50 mM NaOAc, or alternativelyconsisting of 50 mM NaOAc pH 6.0, can follow. Diafiltration for 6-8 DVwill allow for buffer exchange into the desired final formulation bufferof either 10 mM Na₂HPO₄+58 mM sucrose+120 mM NaCl, pH 7.2 or 10 mMcitrate, pH 6.5, and 140 mM NaCl.

In Vitro TF-1 Cell Proliferation Assay for Construct 1997. Method

The in vitro TF-1 cell proliferation assay for the EPO-HSA albuminfusion encoded by construct 1997 was carried out as previously describedin Example 8 under subsection heading “In vitro TF-1 cell proliferationassay for construct 1966”.

Results

Supernatants from NS0 cells expressing construct 1997 were >90% purifiedfor the EPO-HSA albumin fusion protein and were tested in the assay, asdescribed in Example 8. On average, an EC50 of greater than 5 fold ofthat of rhEPO was established (see FIG. 7).

The Activity of Construct 1997 can be Assayed Using an In Vivo HarlanMouse Model for Measuring Hematocrit. Methods

The in vivo Harlan mouse model was used to assay for hematocrit levelsupon subcutaneous administration of either control rhEPO or EPO albuminfusion protein encoded by construct 1981 at various doses on days 0, 2,4, and 6. The assay was carried out as previously described in Example 8under subsection heading “The activity of construct 1966 can be assayedusing an in vivo Harlan mouse model for measuring hematocrit”.Hematocrit was determined on days 0, 8, and 14.

Results

There was a significant and similar increase in hematocrit (see FIG. 8)from day 0 to day 8 for animals treated with either rhEPO or the EPOalbumin fusion encoded by construct 1997. However, as was the case forthe EPO albumin fusion protein encoded by construct 1966 but to a lesserextent, subcutaneous administration of 3 doses/week of 52 μg/kg of EPOalbumin fusion encoded by construct 1997 caused close to 30% change inhematocrit from day 0 to day 8 and subdued to ˜15% on day 14 (see FIG.6) as opposed to a decline from close to 30% to <10% for a triple doseof 12 μg/kg subcutaneous administration of rhEPO per week.

DBA mice injected intravenously with a 150 μg/kg dose of EPO-HSA clearedthis EPO albumin fusion 7 times more slowly than rhEPO.

Example 11 Construct ID 2294, EPO-HSA, Generation

Construct ID 2294, pC4.EPO.R140G.HSA, comprises DNA encoding an EPO-HSAfusion protein which has the full-length EPO protein including thenative leader sequence of the EPO protein, with the exception of thefinal Arg residue, i.e., M1-D192, with a point mutation mutating Arg-140to Gly, fused to the amino-terminus of the mature form of HSA clonedinto the mammalian expression vector pC4.

Cloning of EPO cDNA for Construct 2294.

Construct ID #2294 encodes an albumin fusion protein containing theleader sequence and the mature form of EPO, followed by the mature HSAprotein. Construct ID #2294 was generated by using construct ID #1966,i.e., pC4:EPO.M1-D192.HSA) as a template in a two-step PCR method.

Four oligonucleotides suitable for PCR amplification of thepolynucleotide encoding EPO (SEQ ID NO:X for construct 2294, table 2),EPO7, EPO5, EPO9, and EPO10, were synthesized.

EPO7: (SEQ ID NO: 915) 5′-CTTTGGAT CCGCCACCATGGGGGTGCACGAATGT(primer 82848)-3′ EPO8: (SEQ ID NO: 1123)5′-CCTTCTGGGCTCCCAGAGCCCGAAG (primer 82847)-3′ EPO9: (SEQ ID NO: 916)5′-CATTATCGATGAGCAACCTCACTCTTGTGTGCATCGTCCC (primer 82849)-3′ EPO10:(SEQ ID NO: 1124) 5′-CTTCGGGCTCTGGGAGCCCAGAAGG (primer 82846)-3′

In the first round of PCR amplifications, the N-terminal and theC-terminal fragments of construct ID 1966 were independently amplified.The N-terminal fragment was generated using primers EPO7 and EPO5. EPO7incorporates Bam HI (shown in italics) and has a kozak sequence (shownunderlined) prior to the first 18 nucleotides encoding the first 6 aminoacids of the ORF of the full-length EPO. The EPO8 primer comprises thereverse complement of the sequence spanning amino acids 136 to 143 ofthe full-length form of EPO with the exception that the codon CGAencoding the Arg residue at amino acid 140 (highlighted in bold) isaltered to the codon GGA which encodes a Gly residue. The C-terminalfragment was generated using primers EPO9 and EPO10. In EPO9, theunderlined sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein (SEQ ID NO:1038). In EPO9, thelast 5 nucleotides correspond to the reverse complement of the last 5nucleotides in the full-length EPO, which lacks the final Arg-193residue. The EPO10 primer comprises the nucleic acid sequence encodingamino acids 136 to 143 of the full-length form of EPO with the exceptionthat the codon CGA encoding the Arg residue at amino acid 140(highlighted in bold) is altered to the codon GGA which encodes a Glyresidue. In the second round of PCR amplifications, primers EPO7 andEPO9 were used to amplify the full-length of EPO with the Arg-140 to Glymutation in which the reaction mixture contained both the PCR amplifiedN-terminal fragment and the PCR amplified C-terminal fragment.

The PCR product was purified and then digested with Bam HI and Cla I.After further purification of the Bam HI-Cla I fragment by gelelectrophoresis, the product was cloned into Bam HI Cla I digestedpC4:HSA to give construct ID #2294.

Further, analysis of the N-terminus of the albumin fusion protein byamino acid sequencing can confirm the presence of the expected EPOsequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 2294. Expression in CHOCells.

Construct 2294 can be transfected into CHO cells as described inExamples 6 and 8. Expression levels and specific productivity rates canbe determined as described in Example 8.

Purification from CHO Supernatant.

The cell supernatant containing the EPO-HSA fusion protein expressedfrom construct ID #2294 in CHO cells can be purified as in Examples 7and 8. N-terminal sequencing should yield the sequence APPRLI (SEQ IDNO:2141) which corresponds to the amino terminus of the mature form ofEPO and should yield a protein of approximate MW of 87.7 kDa.

In Vitro TF-1 Cell Proliferation Assay for Construct 2294. Method

The in vitro TF-1 cell proliferation assay for the EPO-HSA albuminfusion encoded by construct 2294 can be carried out as previouslydescribed in Example 8 under subsection heading “In vitro TF-1 cellproliferation assay for construct 1966”.

The Activity of Construct 2294 can be Assayed Using an In Vivo HarlanMouse Model for Measuring Hematocrit.

The in vivo Harlan mouse model as previously described in Example 8under subsection heading, “In vivo Harlan mouse model for measuringhematocrit”, can be used to measure hematocrit levels for the EPOalbumin fusion protein encoded by construct 2294.

Example 12 Construct ID 2298, EPO-HSA, Generation

Construct ID 2298, pEE12.1:EPO.R140G.HSA, comprises DNA encoding an EPOalbumin fusion protein which has the full-length EPO protein (includingthe native leader sequence), with the exception of the final Argresidue, i.e., M1-D192, with a point mutation mutating Arg-140 to Gly,fused to the amino-terminus of the mature form of HSA cloned into themammalian expression vector pEE12.1.

Cloning of EPO cDNA for Construct 2298

Construct ID #2298 encodes an albumin fusion protein containing theleader sequence and the mature form of EPO, followed by the mature HSAprotein. Construct ID #2298 was generated by using construct ID #1997,i.e., pEE12.1:EPO.M1-D192.HSA) as a template for PCR mutagenesis.

Two oligonucleotides suitable for PCR amplification of template ofconstruct ID #1997, EPO11 and EPO12, were synthesized.

EPO11: (SEQ ID NO: 924) 5′-GGCTTCCTTCTGGGCTCCCAGAGCCCGAAGCAG-3′ EPO12:(SEQ ID NO: 923) 5′-CTGCTTCGGGCTCTGGGAGCCCAGAAGGAAGCC-3′

The EPO11 anti-sense primer comprises the reverse complement of thesequence spanning amino acids 135 to 145 of the full-length form of EPOwith the exception that the codon CGA encoding the Arg residue at aminoacid 140 (highlighted in bold) is altered to the codon GGA which encodesa Gly residue. The EPO12 sense primer comprises the nucleic acidsequence encoding amino acids 135 to 145 of the full-length form of EPOwith the exception that the codon CGA encoding the Arg residue at aminoacid 140 (highlighted in bold) is altered to the codon GGA which encodesa Gly residue. Using the Site Directed Mutagenesis kit and protocol fromStratagene, the PCR reaction generated the whole template of constructID #1997 with the exception of the Arg to Gly mutation. The PCR productwas digested with Dpn I, transformed into competent XL1 Blue bacteria,and colonies were sequenced and confirmed. The Dpn I endonuclease isspecific for methylated and hemimethylated DNA and targets the sequence5′-GmATC-3′. Dpn I is used to digest the parental DNA template so as toselect the mutation-containing synthesized DNA.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected EPO sequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 2298.

Expression in NS0 cells.

Construct 2298 can be transfected into NS0 cells as described inExamples 6 and 10. Expression levels and specific productivity rates canbe determined as described in Example 8.

Purification from NS0 Cell Supernatant.

The cell supernatant containing the EPO-HSA fusion protein expressedfrom ID #2298 in NS0 cells can be purified as in Examples 7 and 10.N-terminal sequencing should yield the sequence APPRLI (SEQ ID NO:2141)which corresponds to the amino terminus of the mature form of EPO andshould yield a protein of approximate MW of 87.7 kDa.

In Vitro TF-1 Cell Proliferation Assay for Construct 2298. Method

The in vitro TF-1 cell proliferation assay for the EPO-HSA albuminfusion protein encoded by construct 2298 can be carried out aspreviously described in Example 8 under subsection heading “In vitroTF-1 cell proliferation assay for the albumin-fusion protein encoded byconstruct 1966” and in Example 10 under subsection heading “In vitroTF-1 cell proliferation assay for construct 1997”.

The Activity of Construct 2298 can be Assayed Using an In Vivo HarlanMouse Model for Measuring Hematocrit.

The in vivo Harlan mouse model as previously described in Example 8under subsection heading, “In vivo Harlan mouse model for measuringhematocrit”, and in Example 10 can be used to measure hematocrit levelsfor the EPO albumin fusion protein encoded by construct 2298.

Example 13 Construct ID 2325, EPO-HSA, Generation

Construct ID 2325, pC4.EPO:M1-D192.HSA.codon optimized, comprises DNAencoding an EPO albumin fusion protein which has the full-length EPOprotein (including the native leader sequence), i.e., M1-D192 with theArg-140 to Gly mutation, fused to the amino-terminus of the mature formof HSA cloned into the mammalian expression vector pC4.

Cloning of EPO cDNA for Construct 2325

DNA encoding the EPO open reading frame was codon optimized so as not tohybridize to the wild-type EPO gene sequence. The polynucleotideencoding EPO was PCR generated by 6 overlapping oligonucleotides andcloned into the TA vector. Construct ID #2325 encodes an albumin fusionprotein containing the leader sequence and the mature form of EPO,followed by the mature HSA protein.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected EPO sequence (see below).

EPO albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of EPO lacking the final Arg residue,i.e., Ala-28 to Asp-192. In one embodiment of the invention, EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureEPO albumin fusion protein is secreted directly into the culture medium.EPO albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, EPO albumin fusion proteins of theinvention comprise the native EPO signal sequence. In further preferredembodiments, the EPO albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 2325. Expression in CHOCells.

Construct 2325 can be transfected into CHO cells as described inExamples 6 and 8. Expression levels and specific productivity rates canbe determined as describe in Example 8.

Purification from CHO Supernatant.

The cell supernatant containing the EPO-HSA fusion protein expressedfrom construct ID #2325 in CHO cells can be purified by methodsdescribed in Examples 7 and 8. N-terminal sequencing should yield thesequence APPRLI (SEQ ID NO:2141) which corresponds to the amino terminusof the mature form of EPO and should yield a protein of approximate MWof 87.7 kDa.

In Vitro TF-1 Cell Proliferation Assay for Construct 2325. Method

The in vitro TF-1 cell proliferation assay for the EPO-HSA albuminfusion encoded by construct 2325 can be carried out as previouslydescribed in Example 8 under subsection heading “In vitro TF-1 cellproliferation assay for construct 1966”.

The Activity of Construct 2325 can be Assayed Using an In Vivo HarlanMouse Model for Measuring Hematocrit.

The in vivo Harlan mouse model as previously described in Example 8under subsection heading, “In vivo Harlan mouse model for measuringhematocrit”, can be used to measure hematocrit levels for the EPOalbumin fusion protein encoded by construct 2325.

Example 14 Indications for EPO Albumin Fusion Proteins

Results from in vitro and in vivo assays described above indicate thatEPO albumin fusion proteins can be used in the treatment of bleedingdisorders and anemia caused by a variety of conditions, including butnot limited to: end-stage renal disease (dialysis patients), chronicrenal failure in pre-dialysis, zidovudine-treated HIV patients, cancerpatients on chemotherapy, and premature infants. EPO albumin fusionproteins can also be used pre-surgery in anemic patients undergoingelective non-cardiac, non-vascular surgery to reduce the need for bloodtransfusions. Indications in development for these agents include:aplastic and other refractory anemias, refractory anemia in InflammatoryBowel Disease, and transfusion avoidance in elective orthopedic surgery.Anemia in renal disease and oncology are the two primary indications forEPO albumin fusion proteins encoded by constructs 1966, 1981, 1997,2294, 2298, and 2325.

Example 15 Construct ID 1812, IL2-HSA, Generation

Construct ID 1812, pSAC35:IL2.A21-T153.HSA, comprises DNA encoding anIL2 albumin fusion protein which has an HSA chimeric leader sequence,i.e., the HSA-kex2 signal peptide, the mature IL2 protein, i.e.,A21-T153, fused to the amino-terminus of the mature form of HSA in theyeast S. cerevisiae expression vector pSAC35.

Cloning of IL2 cDNA

The polynucleotide encoding IL2 was PCR amplified using primers IL2-1and IL2-2, described below. The amplimer was cut with Sal I/Cla I, andligated into Xho I/Cla I cut pScCHSA. Construct ID #1812 encodes analbumin fusion protein containing the chimeric leader sequence of HSA,the mature form of IL2, followed by the mature HSA protein.

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the mature form of IL2, IL2-1 and IL2-2, weresynthesized:

IL2-1: (SEQ ID NO: 725) 5′-AGGAGCGTCGACAAAAGAGCACCTACTTCAAGTTCTACAAAG-3′IL2-2: (SEQ ID NO: 726)5′-CTTTAAATCGATGAGCAACCTCACTCTTGTGTGCATCAGTCAGTGT ATGGATGATGCTTTG-3′

IL2-1 incorporates the Sal I cloning site (shown underlined),nucleotides encoding the last three amino acid residues of the HSAchimeric leader sequence, as well as 24 nucleotides encoding the first 8amino acid residues of the mature form of IL2. In IL2-2, the Cla I site(shown underlined) and the DNA following it are the reverse complementof the DNA encoding the first 10 amino acids of the mature HSA protein(SEQ ID NO:1038) and the last 24 nucleotides are the reverse complementof DNA encoding the last 8 amino acid residues of IL2 (see Example 2). APCR amplimer of IL2-HSA was generated using these primers, purified,digested with Sal I and Cla I restriction enzymes, and cloned into theXho I and Cla I sites of the pScCHSA vector. After the sequence wasconfirmed, the expression cassette encoding this IL2 albumin fusionprotein was subcloned into pSAC35 as a Not I fragment.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected IL2 sequence (see below).

IL2 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of IL2, i.e., Ala-21 to Thr-153. In oneembodiment of the invention, IL2 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature IL2 albuminfusion protein is secreted directly into the culture medium. IL2 albuminfusion proteins of the invention may comprise heterologous signalsequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, IL2 albumin fusion proteins of theinvention comprise the native IL2 signal sequence. In further preferredembodiments, the IL2 albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1812.

Expression in Yeast S. cerevisiae.

Transfection of construct 1812 into yeast S. cerevisiae strain BXP10 wascarried out by methods known in the art (see Example 3). Cells werecollected at stationary phase after 72 hours of growth. Supernatantsfrom yeast transfected by construct 1812 were collected by clarifyingcells at 3000g for 10 min. Expression levels were examined by immunoblotdetection with anti-HSA serum (Kent Laboratories) as the primaryantibody. An IL2 albumin fusion protein of approximate molecular weightof 85 kDa was obtained. The specific productivity rates were determinedvia ELISA in which the capture antibody was the US Biological #A1327-35monoclonal anti-HSA antibody or a monoclonal anti-human IL2 antibody(e.g., from Biosource #AHC0422, Pharmingen #555051, R&D Systems #MAB202,or R&D Systems #MAB602), the detecting antibody was a monoclonalanti-human IL2-biotinylated antibody (e.g., from Biosource #AHC069 orEndogen/Pierce #M-600-B) or a monoclonal anti-HSA antibody Biotrend#4T24, respectively, the conjugate was horseradishperoxidase/streptavidin (Vector Laboratories, #SA-5004), and thesubstrate was KPL TMB Peroxidase Substrate (KPL #50-76-01). The analysiswas carried out according to manufacturers' protocol and/or by methodsknown in the art.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing IL2 albumin fusion protein expressedfrom construct ID #1812 in yeast S. cerevisiae cells was purified eithersmall scale over a Dyax peptide affinity column (see Example 4) or largescale by following 5 steps: diafiltration, anion exchange chromatographyusing DEAE-Sepharose Fast Flow column, hydrophobic interactionchromatography (HIC) using Butyl 650S column, cation exchangechromatography using an SP-Sepharose Fast Flow column or aBlue-Sepharose chromatography, and high performance chromatography usingQ-sepharose high performance column chromatography (see Example 4). TheIL2 albumin fusion protein eluted from the DEAE-Sepharose Fast Flowcolumn with 100-250 mM NaCl, from the SP-Sepharose Fast Flow column with150-250 mM NaCl, and from the Q-Sepharose High Performance column at5-7.5 mS/cm. N-terminal sequencing should yield the sequence APTSSSTwhich corresponds to the amino terminus of the mature form of IL2.

The Activity of IL2 can be Assayed Using an In Vitro T and NK Cell-LineProliferation Assay.

The murine CTLL T cell-line is used and is completely dependent on IL2for cell growth and survival. This cell-line expresses high levels ofhigh affinity IL2 receptors and is extremely sensitive to very low dosesof IL2.

Methods

CTLL-2 cells (murine IL2 dependent T cell-line) is grown in RPMI 10% FBScontaining 5 ng/mL recombinant human IL2 and BME. Prior to the assays,the cells are washed twice in PBS to remove IL2. 1×10⁴ cells/well areseeded in a 96-well plate, in a final volume of 200 μl of RPMI 10% FBS.The yeast and 293T supernatants are tested at final concentrations of:10%, 5%, and 1%. In addition, recombinant human IL2, “rhIL2”, is dilutedin the negative control supernatant (HSA alone) to test for the effectof the medium on the stability of the recombinant protein. The cells arecultured at 37° C. for 20 hours, then pulsed with 1 μCi ³H-thymidine for6 hours. Proliferation is measured by thymidine incorporation, eachsample is tested in triplicate.

The Activity of the IL2 Albumin Fusion Protein Encoded by Construct 1812can be Assayed Using an In Vitro T and NK Cell-Line Proliferation Assay.Methods

CTLL-2 cells (murine IL2 dependent T cell-line) was grown in RPMI 10%FBS containing 5 ng/mL recombinant human IL2 and BME. Prior to theassays, the cells were washed twice in PBS to remove IL2. 1×10⁴cells/well were seeded in a 96-well plate, in a final volume of 200 μlof RPMI 10% FBS. The yeast and 293T supernatants were tested at finalconcentrations of: 10%, 5%, and 1%. In addition, recombinant human IL2,“rhIL2”, was diluted in the negative control supernatant (HSA alone) totest for the effect of the medium on the stability of the recombinantprotein. The cells were cultured at 37° C. for 20 hours, then pulsedwith 1 μCi ³H-thymidine for 6 hours. Proliferation was measured bythymidine incorporation, each sample was tested in triplicate.

Results

The IL2 albumin fusion construct ID #1812 stimulated CTLL-2 cellproliferation in a dose-dependent manner (see FIG. 9).

The Activity of the 1L2 Albumin Fusion Protein Encoded by Construct 1812can be Assayed Using an In Vivo BALB/c Model: RENCA Tumor Response toTherapy.

The mouse model employs the RENCA adenocarcinoma of BALB/c mice. TheRENCA tumor used in these studies arose spontaneously. The RENCA tumorswere originally isolated by Dr. Sarah Stewart at the NCI (Bethesda,Md.). RENCA tumors grow progressively following transfer of as few as 50viable cells and spontaneously metastasize from intrarenal implant tothe regional lymph nodes, lungs, liver, and spleen, as well as otherorgans. The immunogenicity of RENCA has been determined to be low tomoderate. RENCA bearing mice routinely die within 35-40 days afterintrarenal injection of 1×10⁵ RENCA tumor cells. Mice given RENCA tumorcells intraperitoneally of a similar number of cells usually die within30-50 days.

Methods

BALB/c mice (6-8 weeks of age) (n=10) were injected subcutaneously inmid-flank with 10⁵ RENCA cells obtained from the fourth in vivo passage.After 10 days of daily (QD) or every other day (QOD) injections withplacebo (PBS), HSA, rhIL2 at a dose of 0.122 mg/kg/QD or at 200,000 or300,000 U/mouse, or IL2 albumin fusion protein at 0.61 mg/kg, mice weremonitored for change in tumor size at days 14, 17, 21, 25, 28, and 31post tumor inoculation. The data are presented in dot-analysis whereeach dot represents single animals. The horizontal line in each grouprepresents MEAN value (see FIG. 10).

Results

IL2 albumin fusion protein encoded by construct ID#1812 was tested inthe above assay.

Administration of IL2 albumin fusion protein expressed from constructID#1812 everyday or every other day showed significant impact on tumorgrowth causing delay of growth and/or shrinkage of tumor size. Everyother day administration was more beneficial since tolerance levels weregreater (see FIG. 10). By day 31 from the inoculation day, 3 micereceiving IL2 albumin fusion products out of 10 were tumor free, only 2showed signs of reduced tumor, and 4 mice had small tumors that appearedto be shrinking. Only one mouse did not respond beneficially to thistreatment. Daily treatment with IL2 albumin fusion protein also caused adelay of growth or actual shrinkage of tumor (2 out of 10 mice weretumor free, 7 remaining mice had small tumors, and 2 had larger ones onthe day of experiment termination). All animals receiving IL2 albuminfusion at 0.61 mg/kg were alive on the termination date, while only 40%of the mice receiving placebo (PBS) and 70% of mice receiving HSA werealive. The biological effect was far more pronounced than therecombinant human IL2 given daily either at 200,000 or 300,000 U/mouse.Recombinant human IL2 had only mediocre effect on tumor growth (all micethat received rhIL2 developed tumors and the only effect observed wasgrowth delay) Of the 10 mice receiving rhIL2 (200,000 or 300,000 U/mL),3 were dead by day 31. The low dose of 0.122 mg/kg/day tested did notinhibit the tumor growth nor spare mice from tumor-related death. TheIL2 albumin fusion protein potently inhibited the in vivo RENCA growthand caused in several cases full recovery from tumors.

Example 16 Construct ID 2030, IL2-HSA, Generation

Construct ID 2030, pSAC35:ycoIL2.A21-T153.HSA, comprises DNA encoding anIL2 albumin fusion protein which has the HSA chimeric leader sequence,i.e., the HSA-kex2 signal peptide, the mature form of the IL2 protein,i.e., A21-T153, fused to the amino-terminus of the mature form of HSA inthe yeast S. cerevisiae expression vector pSAC35.

Cloning of IL2 cDNA

The IL2 open reading frame “ORF” DNA was codon optimized so as not tohybridize to the wild-type IL2 gene. The polynucleotide encoding thecodon optimized IL2 was PCR generated by 6 overlapping oligonucleotidesand cloned into a TA vector. The polynucleotide encoding the codonoptimized IL2 was PCR amplified from this clone using primers IL2-3 andIL2-4, described below, cut with Sal I/Cla I, and ligated into Xho I/ClaI cut pScCHSA. Construct ID #2030 encodes an albumin fusion proteincontaining the chimeric leader sequence of HSA and the mature form ofIL2 fused to the amino terminus of the mature form of HSA.

Two oligonucleotides suitable for PCR amplification of the codonoptimized polynucleotide encoding the mature form of IL2, IL2-3 andIL2-4, were synthesized:

IL2-3: (SEQ ID NO: 831) 5′-AGGAGCGTCGACAAAAGAGCTCCAACTTCTTCTTCTACTAAG-3′IL2-4: (SEQ ID NO: 832)5′-CTTTAAATCGATGAGCAACCTCACTCTTGTGTGCATCTGTCAAAGTAGAAATAATAGA TTGGCAG-3′

IL2-3 incorporates the Sal I cloning site (shown underlined) and encodesfor the last three amino acid residues of the chimeric leader sequenceof HSA, as well as the 24 nucleotides encoding the first 8 amino acidresidues of the mature form of IL2. In IL2-4, the Cla I site (shownunderlined) and the DNA following it are the reverse complement of theDNA encoding the first 10 amino acids of the mature HSA protein (SEQ IDNO:1038) and the last 24 nucleotides are the reverse complement of DNAencoding the last 8 amino acid residues of IL2 (see Example 2). A PCRamplimer was generated using these primers, purified, digested with SalI and Cla I restriction enzymes, and cloned into the Xho I and Cla Isites of the pScCHSA vector. After the sequence was confirmed, the Not Ifragment containing the IL2 albumin fusion protein expression cassettewas subcloned into pSAC35 cut with Not I.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected IL2 sequence (see below).

IL2 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of IL2, i.e., Ala-21 to Thr-153. In oneembodiment of the invention, IL2 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature IL2 albuminfusion protein is secreted directly into the culture medium. IL2 albuminfusion proteins of the invention may comprise heterologous signalsequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, IL2 albumin fusion proteins of theinvention comprise the native IL2 signal sequence. In further preferredembodiments, the IL2 albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 2030.

Expression in Yeast S. cerevisiae.

Transfection into yeast S. cerevisiae strain BXP10 can be carried out bymethods known in the art (see Example 3) and as previously described forconstruct ID 1812 (see Example 15).

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing IL2-HSA expressed from construct ID#2030 in yeast S. cerevisiae cells can be purified either small scaleover a Dyax peptide affinity column (see Example 4) or large scale byfollowing 5 steps: diafiltration, anion exchange chromatography usingDEAE-Sepharose Fast Flow column, hydrophobic interaction chromatography(HIC) using Butyl 650S column, cation exchange chromatography using anSP-Sepharose Fast Flow column or a Blue-Sepharose chromatography, andhigh performance chromatography using Q-sepharose high performancecolumn chromatography (see Example 4 and Example 15). N-terminalsequencing should yield the sequence APTSSST (SEQ ID NO:2142) whichcorresponds to the amino terminus of the mature form of IL2.

The Activity of the IL2 Albumin Fusion Protein Encoded by Construct 2030can be Assayed Using the In Vitro T and NK Cell-Line ProliferationAssay.

The activity of construct ID 2030 can be assayed using an in vitro T andNK cell-line proliferation assay as in Example 15.

The Activity of the IL2 Albumin Fusion Protein Encoded by Construct 2030can be Assayed Using an In Vivo BALB/c Model: RENCA Tumor Response toTherapy.

The activity of the IL2 albumin fusion protein encoded by construct 2030can be assayed using the in vivo BALB/c model as described in Example 15in which the RENCA tumor response to therapy is monitored.

Example 17 Construct ID 2031, HSA-IL2, Generation

Construct ID 2031, pSAC35:HSA.ycoIL2.A21-T153, comprises DNA encoding anIL2 albumin fusion protein which has the HSA full-length sequence thatincludes the HSA chimeric leader sequence, i.e., the HSA-kex2 signalpeptide, fused to the amino-terminus of the mature form of IL2,A21-T153, in the yeast S. cerevisiae expression vector pSAC35.

Cloning of IL2 cDNA

The IL2 open reading frame “ORF” DNA was codon optimized so as not tohybridize to the wild-type IL2 gene. The polynucleotide encoding thecodon optimized IL2 was PCR generated by 6 overlapping oligonucleotidesand cloned into a TA vector. The polynucleotide encoding the codonoptimized IL2 was PCR amplified from this clone using primers IL2-5 andIL2-6, described below, cut with Bsu 36I/Pme I, and ligated into Bsu36I/Pme I cut pScNHSA. Construct ID #2031 encodes an albumin fusionprotein containing the chimeric leader sequence and mature form of HSAand the mature form of IL2.

Two oligonucleotides suitable for PCR amplification of the codonoptimized polynucleotide encoding the mature form of IL2, IL2-5 andIL2-6, were synthesized:

IL2-5: (SEQ ID NO: 833) 5′-AAGCTGCCTTAGGCTTAGCTCCAACTTCTTCTTCTACTAAG-3′IL2-6: (SEQ ID NO: 834)5′-GCGCGCGTTTAAACGGTACCTTATGTCAAAGTAGAAATAATAGATT GGCAG-3′

IL2-5 incorporates the Bsu 36I cloning site (shown underlined) andencodes for the last four amino acid residues of the mature form of HSA,as well as the 24 nucleotides encoding the first 8 amino acid residuesof the mature form of IL2. In IL2-6, the Pme I site is underlined (SEQID NO:834) and the last 24 nucleotides are the reverse complement of DNAencoding the last 8 amino acid residues of IL2 (see Example 2). A PCRamplimer was generated using these primers, purified, digested with Bsu36I and Pme I restriction enzymes, and cloned into the Bsu 36I and Pme Isites of the pScNHSA vector. After the sequence was confirmed, the Not Ifragment containing the IL2 albumin fusion protein expression cassettewas subcloned into pSAC35 cut with Not I.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected HSA sequence (see below).

IL2 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of IL2, i.e., Ala-21 to Thr-153. In oneembodiment of the invention, IL2 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature IL2 albuminfusion protein is secreted directly into the culture medium. IL2 albuminfusion proteins of the invention may comprise heterologous signalsequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, IL2 albumin fusion proteins of theinvention comprise the native IL2 signal sequence. In further preferredembodiments, the IL2 albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 2031.

Expression in Yeast S. cerevisiae.

Transfection into yeast S. cerevisiae strain BXP10 can be carried out bymethods known in the art (see Example 3) and as previously described forconstruct ID 1812 (see Example 15).

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing HSA-IL2 expressed from construct ID#2031 in yeast S. cerevisiae cells can be purified either small scaleover a Dyax peptide affinity column (see Example 4) or large scale byfollowing 5 steps: diafiltration, anion exchange chromatography usingDEAE-Sepharose Fast Flow column, hydrophobic interaction chromatography(HIC) using Butyl 650S column, cation exchange chromatography using anSP-Sepharose Fast Flow column or a Blue-Sepharose chromatography, andhigh performance chromatography using Q-sepharose high performancecolumn chromatography (see Example 4 and Example 15). N-terminalsequencing should yield the sequence DARKS (SEQ ID NO:2143) whichcorresponds to the amino terminus of the mature form of HSA.

The Activity of the IL2 Albumin Fusion Protein Encoded by Construct 2031can be Assayed Using the In Vitro T and NK Cell-Line ProliferationAssay.

The activity of construct ID 2031 can be assayed using an in vitro T andNK cell-line proliferation assay described in Example 15.

The Activity of the IL2 Albumin Fusion Protein Encoded by Construct 2031can be Assayed Using the In Vivo BALB/c Model: RENCA Tumor Response toTherapy.

The activity of the IL2 albumin fusion protein encoded by construct 2031can be assayed using the in vivo BALB/c model as described in Example 15in which the RENCA tumor response to therapy is monitored.

Example 18 Indications for IL2 Albumin Fusion Proteins

Indications for IL2 albumin fusion proteins (including, but not limitedto, those encoded by constructs 1812, 2030, and 2031) include, but arenot limited to, solid tumors, metastatic renal cell carcinoma,metastatic melanoma, malignant melanoma, renal cell carcinoma, HIVinfections treatment (AIDS), inflammatory bowel disorders, Kaposi'ssarcoma, leukemia, multiple sclerosis, rheumatoid arthritis, transplantrejection, type I diabetes mellitus, lung cancer, acute myeloidleukemia, hepatitis C, non-Hodgkin's Lymphoma, and ovarian cancer.

Example 19 Construct ID 1642, GCSF-HSA, Generation

Construct ID 1642, pSAC35:GCSF.T31-P204.HSA, comprises DNA encoding aGCSF albumin fusion protein which has the HSA chimeric leader sequence,i.e., the HSA-kex2 signal peptide, the mature form of the “short form”of Granulocyte Colony Stimulating Factor, “G-CSF”, protein, i.e.,T31-P204, fused to the amino-terminus of the mature form of HSA in theyeast S. cerevisiae expression vector pSAC35.

Cloning of GCSF cDNA

A polynucleotide encoding GCSF was PCR amplified using primers GCSF-1and GCSF-2, described below. The amplimer was cut with Sal I/Cla I, andligated into Xho I/Cla I cut pScCHSA. Construct ID #1642 comprises DNAwhich encodes an albumin fusion protein containing the chimeric leadersequence of HSA, the mature form of GCSF, followed by the mature HSAprotein.

Two oligonucleotides suitable for PCR amplification of a polynucleotideencoding the mature form of GCSF, GCSF-1 and GCSF-2, were synthesized:

GCSF-1: (SEQ ID NO: 665) 5′-GAATTCGTCGACAAAAGAACCCCCCTGGGCCCTGCCAG-3′GCSF-2: (SEQ ID NO: 666)5′-AAGCTTATCGATGAGCAACCTCACTCTTGTGTGCATCGGGCTGGGC AAGGTGGCGTAG-3′

GCSF-1 incorporates the Sal I cloning site (shown underlined),nucleotides encoding the last three amino acid residues of the HSAchimeric leader sequence, as well as 20 nucleotides encoding the first 6amino acid residues of the mature form of GCSF. In GCSF-2, the Cla Isite (shown underlined) and the DNA following it are the reversecomplement of the DNA encoding the first 10 amino acids of the matureHSA protein (SEQ ID NO:1038) and the last 21 nucleotides are the reversecomplement of DNA encoding the last 7 amino acid residues of GCSF. Usingthese primers, a PCR amplimer was generated, purified, digested with SalI and Cla I restriction enzymes, and cloned into the Xho I and Cla Isites of the pScCHSA vector. After the sequence was confirmed, the Not Ifragment containing the GCSF albumin fusion expression cassette wassubcloned into pSAC35 cut with Not I.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedGCSF sequence (see below).

GCSF albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of GCSF, i.e., Thr-31 to Pro-204. In oneembodiment of the invention, GCSF albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature GCSF albuminfusion protein is secreted directly into the culture medium. GCSFalbumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, GCSF albumin fusion proteins of theinvention comprise the native GCSF signal sequence. In further preferredembodiments, the GCSF albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1642.

Expression in Yeast S. cerevisiae.

Transformation of construct 1642 into yeast S. cerevisiae strains D88,BXP10, and DXY1—a YAP3 mutant, was carried out by methods known in theart (see Example 3). A preliminary “Halo Assay” was carried out toassess if the transformed yeast are producing the proteins encoded bythe fusion constructs. Secretion of HSA fusion proteins into agar mediacontaining anti-HSA antibodies will result in the formation of aninsoluble “precipitin” ring or halo. The size of the halo isproportional to the amount of HSA protein being produced.LEU2+prototrophs were selected on synthetic complete leucine dropoutmedium containing dextrose, “SCD-Leu”. Selected colonies as well as apositive control were gridded onto a BMMD plate containing anti-HSAantibody. After growth, the plates were incubated at 4° C. to allow forprecipitin ring formation. Based on the “Halo Assay”, colonies fromtransformation of construct 1642 produced protein. To establish theextent of secretion, transformed cells were collected at stationaryphase after 48 hours of growth in suspension. Supernatants werecollected by clarifying cells at 3000 g for 10 min. Expression levelswere examined by immunoblot detection with anti-HSA serum (KentLaboratories) or with an antibody directed to the Therapeutic proteinportion, i.e., GCSF, of the albumin fusion protein. The GCSF albuminfusion protein of approximate molecular weight of 88 kDa was obtained.To obtain workable quantities for purification, the yeast transformantswere inoculated in 1 L of BMM media at 150 rpm, 29.5° C. The culture wascentrifuged and passed through a 0.45 □m filter. The specificproductivity rates can be determined via ELISA in which, for example,the capture antibody is the R&D Systems Clone 3316.111 monoclonal mouseanti-GCSF, the detecting antibody is the R&D Systems BAF214 (i.e., CloneACN030081) biotinylated goat anti-human GCSF antibody, the conjugate ishorseradish peroxidase/streptavidin (Vector Laboratories, #SA-5004), andthe substrate is KPL TMB Peroxidase Substrate (KPL #50-76-01), where theanalysis is carried out according to manufacturers' protocol and/or bymethods known in the art.

Purification from Yeast S. cerevisiae Cell Supernatant.

A general purification procedure for albumin fusion proteins has beendescribed in Example 4. The purification of GCSF albumin fusion proteinis described specifically below. Another purification scheme isdescribed in Example 20.

Step 1: Phenyl Fast Flow Chromatography (Amersham Pharmacia Biotech)

The yeast culture supernatant (3 L) containing GCSF-HSA encoded byconstruct 1642 was loaded onto a phenyl fast flow column with 1 M ofammonium sulfate in 50 mM Tris, pH 7.2. The column was washed with 1 Mof ammonium sulfate in 50 mM Tris, pH 7.2, 0.2 M ammonium sulfate in 50mM Tris, pH 7.2, and then washed with the buffer. The GCSF-HSA fusionprotein was eluted with water (Water For Injection distilled water WFI).

Step 2: SP Fast Flow Chromatography (Amersham Pharmacia Biotech)

The eluate of Step 1 was mixed with an equal volume of a solutioncomposed of 10.3 mM Na₂HPO₄ and 4.85 mM citric acid, pH 5.0. The mixturewas loaded at 300 cm/hr onto a SP fast flow column and eluted with asolution composed of 0.5 M NaCl in 10.3 mM Na₂HPO₄ and 4.85 mM citricacid, pH 5.0. The column was then stripped with a solution composed of1M NaCl in 10.3 mM Na₂HPO₄ and 4.85 mM citric acid, pH 5.0.

Step 3: Methyl HIC Chromatography (BioRad)

The eluate of Step 2 was titrated to a final concentration of 1 Mammonium sulfate (143 mS) in 50 mM Tris, pH 7.2 and loaded onto methylHIC column. The column was washed to a baseline, then washed with 0.6 Mammonium sulfate in 50 mM Tris, pH 7.2. A gradient from 0.6 M ammoniumsulfate to 0 M ammonium sulfate was initiated. The column was finallystripped with WFI and 0.5 M NaOH. A lot of the impurities in the sampleeluted at the lower ammonium sulfate concentrations thereby affordingthe GCSF-HSA fusion high purity.

Step 4: CM Fast Flow Chromatography (Amersham Pharmacia Biotech)

The eluate of Step 3 was diluted with WFI to 5 mS, pH 5.5 and was loadedonto the CM column at 300 cm/hr. The column was eluted with 0.5 M NaClin 11 mM Na₂HPO₄ and 4 mM citric acid, pH 5.5. The column was strippedwith 1 M NaCl in 11 mM Na₂HPO₄ and 4 mM citric acid, pH 5.5.

Step 5: Ultrafiltration/Diafiltration (Amersham Pharmacia Biotech)

The purified product was ultrafiltered and diafiltered into PhosphateBuffered Saline, “PBS”, pH 7.2.

The purified GCSF albumin fusion protein encoded by construct 1642 wasanalyzed for purity on SDS/PAGE. It was >95% pure. The protein wassequenced confirmed and also showed 90% purity on N-terminal sequencingwith an N-terminal sequence of “TPLGP” (SEQ ID NO:2144).

The Activity of GCSF can be Assayed Using an In Vitro NFS-60 CellProliferation Assay. Method

To assess GCSF activity, NSF-60 cells, a myeloid factor-dependentcell-line derived from Primary Lake Cascitus wild ecotropicvirus-induced tumor of NFS mice, are employed.

Cell Growth and Preparation

Cells are originally seeded in T-75 cm² flasks at approximately 1.5×10⁴cells/mL in growth media (RPMI 1640 containing 10% Fetal Bovine Serum,“FBS”, 1× Penicillin/Streptomycin, 1× L-Glutamine (final concentrationof 2 mM), and recombinant murine interleukin-3, (IL3) at 30 ng/mL).Cells are split anywhere from 1:10 to 1:20 every 2 days and reseeded infresh medium.

NFS-60 Bioassay

The NFS-60 assay is performed as described in Weinstein et al.(Weinstein et al., 1986, Proc. Natl. Acad. Sci. USA, 83, pp 5010-4).Briefly, the day before the assay is to be performed, cells are reseededto 1.0×10⁵ in fresh assay growth medium containing IL3. The next daycells are transferred to 50 mL conical tubes, centrifuged at low speeds,and washed twice in plain RPMI without serum or growth factors. Thepellet is resuspended in 25 mL and the cells are subsequently counted.The cells are spun once more and resuspended at the workingconcentration in growth medium (described above) but lacking IL3. Thecells are plated in 96-well round-bottom TC-treated plates at 1×10⁵cells/well. Increasing doses of GCSF are added to each well to a finalvolume of 0.1 mL. The assay is done in triplicate. The cells arecultured for 24 hours to determine the level of cell proliferation.³H-Thymidine (5 μCi/mL) is added 4 hours prior to the experimenttermination. The cells are then harvested on glass fiber filters using acell harvester and the amount of ³H-Thymidine labeled DNA is countedusing TOP-Count.

The Activity of GCSF Albumin Fusion Encoded by Construct ID #1642 can beAssayed Using an In Vitro NFS-60 Cell Proliferation Assay. Method

GCSF albumin fusion protein encoded by construct 1642 was tested in thein vitro NFS-60 cell proliferation bioassay described above.

Cell Growth and Preparation

Cells were prepared as described above.

NFS-60 Bioassay

The day before the assay was performed, cells were reseeded to 1.0×10⁵in fresh assay growth medium containing IL3. The next day cells weretransferred to 50 mL conical tubes, centrifuged at low speeds, andwashed twice in plain RPMI without serum or growth factors. The pelletwas resuspended in 25 mL and the cells were subsequently counted. Thecells were spun once more and resuspended at the working concentrationin growth medium (described above) but lacking IL3. The cells wereplated in 96-well round-bottom TC-treated plates at 1×10⁵ cells/well.Increasing doses either of HSA, recombinant human GCSF (rhGCSF), or apartially purified GCSF albumin fusion protein from the yeastsupernatant, were added to individual wells to a final volume of 0.1 mL.The assay was done in triplicate. The cells were cultured for 24 hoursto determine the level of cell proliferation. ³H-Thymidine (5 □Ci/mL)was added 4 hours prior to the experiment termination. The cells werethen harvested on glass fiber filters using cell harvester and theamount of ³H-Thymidine labeled DNA was counted using TOP-Count.

Results

Construct 1642 demonstrated NFS-60 cell proliferation activity in a dosedependent manner, while the control supernatant from yeast expressingHSA alone did not produce any activity (see FIG. 11).

The Activity of GCSF can be Assayed In Vivo Using C57BL/6 Mice: GCSF asa Mobilizing Agent.

G-CSF is capable of mobilizing granulocytes to the periphery as well asincreasing the total White Blood Cell, (WBC), count when administered tomice. Recombinant human GCSF, (rhGCSF), cross-reacts with recombinantmurine GCSF, (rmGCSF).

Methods

Mice are ear tagged before the injections start. Mice are injectedintraperitoneally with rhGCSF (Neupogen, AMEN) at either 5 □g (n=5) or10 □g (n=5) twice a day for 7 consecutive days. The control mice (n=3)receive Hepes Buffered Saline Solution, (HBSS). At 24 hours after thelast rhGCSF administration, peripheral blood is drawn from the tail andanalysed for the granulocyte content and total WBC count.

Results

Both doses of rhGCSF efficiently increase both the frequency and thetotal number of granulocytes as well as the total WBC count (see FIG.12). This effect is apparent after 24 hours of the final rhGCSFintraperitoneal administration. This effect is transient and the numberof granulocytes return to normal values by day 5.

The Activity of GCSF Albumin Fusion Protein Encoded by Construct ID#1642 can be Assayed In Vivo Using C57BL/6 Mice: GCSF-HSA as aMobilizing Agent. Methods

The GCSF albumin fusion protein encoded by construct 1642 can be assayedaccording to the procedure described above. Briefly, mice are to be eartagged before the injections are to begin. Mice are to be injectedintraperitoneally with either rhGCSF, as a control, or the GCSF albuminfusion protein at either 5 □g (n=5) or 10 □g (n=5) twice a day for 7consecutive days. Additional control mice (n=3) are to receive HepesBuffered saline Solution, “HBSS”. At 24 hours after the last GCSFadministration, peripheral blood can be drawn from the tail and analysedfor the granulocyte content and total WBC count.

Example 20 Construct ID 1643, HSA-GCSF, Generation

Construct ID 1643, pSAC35:HSA.GCSF.T31-P204, comprises DNA encoding aGCSF albumin fusion protein which has the full-length HSA protein thatincludes the HSA chimeric leader sequence, i.e., the HSA-kex2 signalpeptide, fused to the amino-terminus of the mature form of the GCSFprotein, i.e., A21-T153, in the yeast S. cerevisiae expression vectorpSAC35.

Cloning of GCSF cDNA

The polynucleotide encoding GCSF was PCR amplified using primersGCSF-3and GCSF-4, described below. The amplimer was cut with Bsu 36I/AscI, and ligated into Bsu 36I/Asc I cut pScNHSA. Construct ID #1643encodes an albumin fusion protein containing the chimeric leadersequence and mature form of HSA and the mature form of GCSF.

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the mature form of GCSF, GCSF-3 and GCSF-4, weresynthesized:

GCSF-3: (SEQ ID NO: 667) 5′-AAGCTGCCTTAGGCTTAACCCCCCTGGGCCCTGCCAG-3′GCSF-4: (SEQ ID NO: 668) 5′-GCGCGCGGCGCGCCTCAGGGCTGGGCAAGGTGGCGTAG-3′

GCSF-3 incorporates the Bsu 36I cloning site (shown underlined) andnucleotides encoding the last four amino acid residues of the matureform of HSA, as well as 20 nucleotides encoding the first 6 amino acidresidues of the mature form of GCSF. In GCSF-4, the Asc I site isunderlined and the last 24 nucleotides are the reverse complement of DNAencoding the last 8 amino acid residues of GCSF. A PCR amplimer ofHSA-GCSF was generated using these primers, purified, digested with Bsu36I and Asc I restriction enzymes, and cloned into the Bsu 36I and Asc Isites of the pScNHSA vector. After the sequence was confirmed, theexpression cassette encoding this GCSF albumin fusion protein wassubcloned into pSAC35 as a Not I fragment.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedHSA sequence (see below).

GCSF albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of GCSF, i.e., Thr-3 1 to Pro-204. In oneembodiment of the invention, GCSF albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature GCSF albuminfusion protein is secreted directly into the culture medium. GCSFalbumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, GCSF albumin fusion proteins of theinvention comprise the native GCSF signal sequence. In further preferredembodiments, the GCSF albumin fusion proteins of the invention furthercomprise an N-terminal methionine residue. Polynucleotides encodingthese polypeptides, including fragments and/or variants, are alsoencompassed by the invention.

Expression and Purification of Construct ID 1643.

Expression in Yeast S. cerevisiae.

Transformation of construct 1643 into yeast S. cerevisiae was carriedout by methods known in the art (see Example 3) and as previouslydescribed for construct ID 1642 (see Example 19).

Purification from Yeast S. cerevisiae Cell Supernatant.

A general procedure for purification of albumin fusion proteins isdescribed in Example 4. The cell supernatant containing GCSF albuminfusion protein expressed from construct ID #1643 in yeast S. cerevisiaecells was purified according to the following method. Anotherpurification scheme is described in Example 19.

Step 1: Phenyl Sepharose Fast Flow (Hs), pH 7.2

The fermentation supernatant (3.5 L) was adjusted to 139 mS and pH 7.2with ammonium sulfate to a final concentration of 1 M in 50 mM Tris, pH7.2. The phenyl sepharose column was loaded at a flow rate of 300 cm/hr.The column was washed with 50 mM Tris-HCl, pH 7.2. A series of lowersalt elutions were executed to remove contaminating proteins followed bya WFI elution to elute the target protein. A NaOH strip of the columnrevealed that a significant portion of the target protein was notremoved by previous treatments.

Step 2: Mimetic Blue, pH 6.5

The eluted target protein was diafiltered with 20 mM citrate phosphatebuffer, (CPB), pH 6.5 and then loaded onto a Mimetic Blue columnpreviously equilibrated with 20 mM CPB, pH 6.5 buffer. The column waswashed with equilibration buffer for 10 column volumes. The majority ofthe target protein was then eluted with a 0.2 M NaCl wash. Higher saltconcentration elution solutions (1 M and 2 M NaCl) revealed some targetprotein. However, when HPLC-SEC was performed on these fractions themajority of the target protein was observed as aggregates. Thispurification step resulted in >85% purity of the target protein.

Step 3: Q HP, pH 6.5

The target protein was diluted with 20 mM CPB, pH 6.5 (5-fold) to aconductivity of <5 mS and loaded onto the Q HP resin. A series ofelutions, 100 mM, 200 mM, 500 mM, and 1 M NaCl, were performed. Thetarget protein eluted with 100 mM NaCl.

Step 4: SP FF, pH 5.5

The target protein was diluted with 20 mM CPB, pH 5.0, and adjusted topH 5.0. The target protein was loaded onto SP Sepharose FF column. Thecolumn was washed with 5 column volumes of equilibration buffer. The 45kDa contaminating protein, a proteolyzed fragment of HSA, did not bindto the resin and was observed in the load flow thru (LFT). The targetprotein was eluted in a shallow gradient from 0-500 mM NaCl. The targetprotein eluted at about 250 mM NaCl. The target protein was diafilteredinto the final storage buffer of 20 mM CPB, pH 6.5.

Analysis by SDS-PAGE identified an 88 kDa protein with >95% purity.N-terminal sequencing resulted in the major sequence being “DAHKS” (SEQID NO:2143) which is the amino-terminus of the mature form of HSA. Thefinal buffer composition is 20 mM CPB, pH 6.5. From 3.5 L of culturesupernatant, 1.94 mg protein was purified.

The Activity of GCSF Albumin Fusion Encoded by Construct ID #1643 can beAssayed Using an In Vitro NFS-60 Cell Proliferation Assay. Method

The GCSF albumin fusion protein encoded by construct 1643 was tested inthe in vitro NFS-60 cell proliferation bioassay previously described inExample 19 under subsection headings, “The activity of GCSF can beassayed using an in vitro NFS-60 cell proliferation assay” and “Theactivity of GCSF albumin fusion encoded by construct ID #1642 can beassayed using an in vitro NFS-60 cell proliferation assay”.

Results

Construct 1643 demonstrated the ability to cause NFS-60 cellproliferation in a dose dependent manner, while the control supernatantwith HSA alone did not produce any activity (see FIG. 11).

The Activity of GCSF Albumin Fusion Encoded by Construct ID #1643 can beAssayed In Vivo Using C57BL/6 Mice: GCSF-HSA as a Mobilizing Agent.Methods

The GCSF albumin fusion protein encoded by construct 1643 can be assayedaccording to the procedure as previously described in Example 19 undersubsection headings, “The activity of GCSF can be assayed in vivo usingC57BL/6 mice: GCSF-HSA as a Mobilizing Agent” and “The activity of GCSFalbumin fusion encoded by construct ID #1642 can be assayed in vivousing C57BL/6 mice: GCSF-HSA as a Mobilizing Agent”.

Example 21 Indications for GCSF Albumin Fusion Proteins

Based on the activity of GCSF albumin fusion proteins in the aboveassays, GCSF albumin fusion proteins are useful in chemoprotection,treating, preventing, and/or diagnosing inflammatory disorders,myelocytic leukemia, primary neutropenias (e.g., Kostmann syndrome),secondary neutropenia, prevention of neutropenia, prevention andtreatment of neutropenia in HIV-infected patients, prevention andtreatment of neutropenia associated with chemotherapy, infectionsassociated with neutropenias, myelopysplasia, and autoimmune disorders,mobilization of hematopoietic progenitor cells, bone marrow transplant,acute myelogeneous leukemia, non-Hodgkin's lymphoma, acute lymphoblasticleukemia, Hodgkin's disease, accelerated myeloid recovery, and glycogenstorage disease.

Example 22 Construct ID 2363, GCSF-HSA-EPO.A28-D192, Generation

Construct ID 2363, pC4:GCSF.HSA.EPO.A28-D192, comprises DNA encoding aGCSF-HSA-EPO triple fusion protein having the full-length form of theGranulocyte Colony Stimulating Factor, (G-CSF), protein, fused to theamino-terminus of the mature form of HSA, which is fused to theamino-terminus of the mature form of EPO, i.e., amino acids A28-D192,with the exception of the final Arg residue, in the CHO mammaliancell-line expression vector pC4.

Cloning of GCSF-HSA-EPO cDNA

Construct ID #1642, i.e., pSAC35:GCSF.T31-P204.HSA (Example 19), wasused as a template to generate a part of construct 2363. The followingpolynucleotides were synthesized:

GCSF/EPO-1: (SEQ ID NO: 1129) 5′-TGTGGCACAGTGCACTCTGGACAGTGCAGGAAGCCACCCCCCTGGGCCCTGCCAGCTCCC-3′ (primer 79388) GCSF/EPO-2: (SEQ ID NO: 1130)5′-GGCACACTTGAGTCTCTGTTTGGCAGACG-3′ (primer 79239) GCSF/EPO-3:(SEQ ID NO: 1131) 5′-ACCCAGAGCCCCATGAAGCTGATGGCCCTGCAGCTGCTGCTGTGGCACAGTGCACTCTGG-3′ (primer 79389) GCSF/EPO-4: (SEQ ID NO: 1132)5′-GGTTGGGATCCAAGCTTCCGCCACCATGGCTGGACCTGCCACCCAGAGCCCCATGAAGCT-3′(primer 79390)

The full-length sequence of GCSF was generated in a three-stepoverlapping PCR reaction using combinations of primers GCSF/EPO-1,GCSF/EPO-2, GCSF/EPO-3, and GCSF/EPO-4. Primers GCSF/EPO-1, GCSF/EPO-3,and GCSF/EPO-4 consist of sequences that span the amino-terminus of thefull-length of GCSF. Primer GCSF/EPO-2 comprises of the reversecomplement of the sequence that spans amino acids Ser-216 to Ala-225 ofHSA. The first PCR reaction included construct 1642 as template andprimers GCSF/EPO-1 and GCSF/EPO-2. The product obtained from the firstPCR reaction was used as template in the second PCR reaction whichincluded primers GCSF/EPO-3 and GCSF/EPO-2. The product obtained fromthe second PCR reaction was used as template in the third PCR reactionwhich included primers GCSF/EPO-4 and GCSF/EPO-2. Primer GCSF/EPO-4 hasa Bam HI site (shown in italics) followed by the Kozak sequence (shownunderlined). The final PCR product contains a 5′ Bam HI restriction sitefollowed by an appropriate Kozak sequence, the entire full-length GCSFcoding sequence and part of the HSA open reading frame fromAsp-25-Ala-225. The Cla I site is inherent in the polynucleotidesequence of the mature form of HSA and is localized in close proximityto the 5′-end of the mature form of HSA. The Bam HI-Cla I fragment wascloned into similarly digested pC4.HSA.EPO.A28-D192 construct ID #1981.

Construct ID #2363 encodes an albumin fusion protein containing theleader and mature forms of GCSF, followed by the mature HSA protein,followed by the mature form of EPO.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected GCSF sequence (see below).

GCSF/EPO albumin fusion proteins of the invention preferably comprisethe mature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N-or C-terminus of the mature form of GCSF, i.e., Thr-31 to Pro-204, andfused to either the N- or C-terminus of the mature form of EPO, i.e.,Ala-28 to Asp-192. In one embodiment of the invention, GCSF/EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureGCSF/EPO albumin fusion protein is secreted directly into the culturemedium. GCSF/EPO albumin fusion proteins of the invention may compriseheterologous signal sequences including, but not limited to, MAF, INV,Ig, Fibulin B, Clusterin, Insulin-Like Growth Factor Binding Protein 4,variant HSA leader sequences including, but not limited to, a chimericHSA/MAF leader sequence, or other heterologous signal sequences known inthe art. In a preferred embodiment, GCSF/EPO albumin fusion proteins ofthe invention comprise either the native GCSF or the native EPO signalsequence. In further preferred embodiments, the GCSF/EPO albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Expression and Purification of Construct ID 2363. Expression in CHOCells.

Construct 2363 can be transfected into CHO cells as previously describedin Examples 6 and 8.

Purification from CHO Supernatant.

A general purification procedure for albumin fusion proteins has beendescribed in Example 7. The triple fusion protein GCSF-HSA-EPO encodedby construct 2363 can be purified as previously described in Examples 7and 9. N-terminal sequencing should yield the sequence TPLGP (SEQ IDNO:2144) which corresponds to the mature form of GCSF.

The Activity of GCSF-HSA-EPO Encoded by Construct ID #2363 can beAssayed Using an In Vitro TF-1 Cell Proliferation Assay and an In VitroNFS-60 Cell Proliferation Assay. Method

The activity of the triple fusion protein GCSF-HSA-EPO encoded byconstruct 2363 was assayed in the in vitro TF-1 cell proliferation assayas previously described under subsection heading, “In vitro TF-1 cellproliferation assay for construct 1981”, in Example 9, as well as in thein vitro NFS-60 cell proliferation assay as previously described undersubsection heading, “The activity of GCSF albumin fusion encoded byconstruct ID #1642 can be assayed using an in vitro NFS-60 cellproliferation assay”, in Example 19.

Result

THE GCSF-HSA-EPO albumin fusion encoded by construct 2363 demonstratedproliferation of both TF-1 cells and NFS-60 cells.

The Activity of GCSF-HSA-EPO Albumin Fusion Encoded by Construct ID#2363 can be Assayed In Vivo.

The activity of the triple fusion protein GCSF-HSA-EPO encoded byconstruct 2363 can be assayed in the in vivo Harlan mouse model tomeasure hematocrit levels as previously described in Example 9 undersubsection heading, “The activity of construct 1981 can be assayed usingan in vivo Harlan mouse model for measuring hematocrit”, as well as inC57BL/6 mice where GCSF-HSA-EPO is a mobilizing agent as previouslydescribed in Example 19 under subsection heading, “The activity of GCSFalbumin fusion encoded by construct ID #1642 can be assayed in vivousing C57BL/6 mice: GCSF-HSA as a Mobilizing Agent”.

Example 23 Construct ID 2373, GCSF-HSA-EPO.A28-D192, Generation

Construct ID 2373, pC4:GCSF.HSA.EPO.A28-D192.R140G, comprises DNAencoding a GCSF-HSA-EPO triple fusion protein which has the full-lengthform of the Granulocyte Colony Stimulating Factor, “G-CSF”, protein,fused to the amino-terminus of the mature form of HSA, which is fused tothe amino-terminus of the mature form of EPO, i.e., A28-D192 which hasthe Arg-140 to Gly mutation, in the CHO mammalian cell-line expressionvector pC4.

Cloning of EPO cDNA for Construct 2373

Construct ID #2373 encodes an albumin fusion protein containing theleader sequence and the mature form of GCSF, followed by the mature HSAprotein followed by the mature form of EPO which has the Arg-140 to Glymutation (SEQ ID NO:401). Construct ID #2373 was generated by usingconstruct ID #2363, i.e., pC4:GCSF.HSA.EPO.R140G as a template for PCRmutagenesis.

Four oligonucleotides suitable for PCR amplification of template ofconstruct ID #2363, GCSF/EPO-5, GCSF/EPO-6, GCSF/EPO-7, and GCSF/EPO-8,were synthesized.

GCSF/EPO-5: (SEQ ID NO: 1125) 5′-GTTGAAAGTAAGGATGTTTG-3′ (primer 78219)GCSF/EPO-6: (SEQ ID NO: 1126) 5′-CCTTCTGGGCTCCCAGAGCCCGAAG-3′(primer 82847) GCSF/EPO-7: (SEQ ID NO: 1127)5′-CTTCGGGCTCTGGGAGCCCAGAAGG-3′ (primer 82846) GCSF/EPO-8:(SEQ ID NO: 1128) 5′-ACCAGGTAGAGAGCTTCCACC-3′ (pC3′)

Construct 2373 was generated by nested PCR amplification using construct2363 as the template. In the first round of PCR amplifications, theN-terminal and the C-terminal fragments of construct ID 2363 wereindependently amplified. The N-terminal fragment was generated usingprimers GCSF/EPO-5 and GCSF/EPO-6. The GCSF/EPO-5 corresponds to thenucleic acid sequence that encodes for amino acid residues 334 to 340 ofthe full-length form of HSA. The GCSF/EPO-6 primer comprises the reversecomplement of the sequence spanning amino acids 136 to 143 of thefull-length form of EPO with the exception that the codon CGA encodingthe Arg residue at amino acid 140 (highlighted in bold) is altered tothe codon GGA which encodes a Gly residue. The C-terminal fragment wasgenerated using primers GCSF/EPO-7 and GCSF/EPO-8. The GCSF/EPO-7 primercomprises the nucleic acid sequence encoding amino acids 136 to 143 ofthe full-length form of EPO with the exception that the codon CGAencoding the Arg residue at amino acid 140 (highlighted in bold) isaltered to the codon GGA which encodes a Gly residue. In GCSF/EPO-8, thesequence comprises nucleotides within the pC4 vector downstream of thestop codon. In the second round of PCR amplifications, primersGCSF/EPO-5 and GCSF/EPO-8 were used to amplify the GCSF-HSA-EPO triplefusion protein which has the full-length form of G-CSF fused to theamino-terminus of the mature form of HSA, which is fused to theamino-terminus of the mature form of EPO, i.e., A28-D192 which has theArg-140 to Gly mutation. The reaction mixture contained both the PCRamplified N-terminal fragment and the PCR amplified C-terminal fragment.

The PCR product was purified and then digested with Bsu36I and AscI.After further purification of the Bsu36I-AscI fragment by gelelectrophoresis, the product was cloned into Bsu36I/AscI digestedconstruct 2363 to give construct ID #2373.

Further, analysis of the N-terminus of the albumin fusion protein byamino acid sequencing can confirm the presence of the expected GCSFsequence (see below).

GCSF/EPO albumin fusion proteins of the invention preferably comprisethe mature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N-or C-terminus of the mature form of GCSF, i.e., Thr-31 to Pro-204, andfused to either the N- or C-terminus of the mature form of EPO, i.e.,Ala-28 to Asp-192. In one embodiment of the invention, GCSF/EPO albuminfusion proteins of the invention further comprise a signal sequencewhich directs the nascent fusion polypeptide in the secretory pathwaysof the host used for expression. In a further preferred embodiment, thesignal peptide encoded by the signal sequence is removed, and the matureGCSF/EPO albumin fusion protein is secreted directly into the culturemedium. GCSF/EPO albumin fusion proteins of the invention may compriseheterologous signal sequences including, but not limited to, MAF, INV,Ig, Fibulin B, Clusterin, Insulin-Like Growth Factor Binding Protein 4,variant HSA leader sequences including, but not limited to, a chimericHSA/MAF leader sequence, or other heterologous signal sequences known inthe art. In a preferred embodiment, GCSF/EPO albumin fusion proteins ofthe invention comprise either the native GCSF or the native EPO signalsequence. In further preferred embodiments, the GCSF/EPO albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Expression and Purification of Construct ID 2373. Expression in CHOCells.

Construct 2373 can be transfected into CHO cells as previously describedin Examples 6 and 8.

Purification from CHO Supernatant.

A general purification procedure for albumin fusion proteins has beendescribed in Example 7. The triple fusion protein GCSF-HSA-EPO.R140Gencoded by construct 2373 can be purified as previously described inExamples 7 and 8. N-terminal sequencing should yield the sequence TPLGP(SEQ ID NO:2144) which corresponds to the mature form of GCSF.

The Activity of GCSF-HSA-EPO.R140G Encoded by Construct ID #2373 can beAssayed Using an In Vitro TF-1 Cell Proliferation Assay and an In VitroNFS-60 Cell Proliferation Assay. Method

The activity of the triple fusion protein GCSF-HSA-EPO.R140G encoded byconstruct 2373 can be assayed in the in vitro TF-1 cell proliferationassay as previously described in Example 9 under subsection heading, “Invitro TF-1 cell proliferation assay for construct 1981”, as well as inthe in vitro NFS-60 cell proliferation assay as previously described inExample 19 under subsection heading, “The activity of GCSF albuminfusion encoded by construct ID #1642 can be assayed using an in vitroNFS-60 cell proliferation assay”.

Result

THE GCSF-HSA-EPO.R140G albumin fusion encoded by construct 2373demonstrated proliferation of both TF-1 cells and NFS-60 cells.

The Activity of GCSF-HSA-EPO.R140G Albumin Fusion Encoded by ConstructID #2373 can be Assayed In Vivo. Method

The activity of the triple fusion protein GCSF-HSA-EPO.R140G encoded byconstruct 2373 can be assayed in the in vivo Harlan mouse model tomeasure hematocrit levels as previously described in Example 9 undersubsection heading, “The activity of construct 1981 can be assayed usingan in vivo Harlan mouse model for measuring hematocrit”, as well as inC57BL/6 mice where GCSF-HSA-EPO.R140G is a mobilizing agent aspreviously described in Example 19 under subsection heading, “Theactivity of GCSF albumin fusion encoded by construct ID #1642 can beassayed in vivo using C57BL/6 mice: GCSF-HSA as a Mobilizing Agent”.

Example 24 Indications for the GCSF-HSA-EPO Triple Fusion

Indications for triple fusion proteins comprising GCSF, EPO and HSA,(including, but not limited to, those encoded by constructs 2363 and2373) may include those indications specified for the EPO albumin fusionproteins and for the GCSF albumin fusion proteins, including but notlimited to, bleeding disorders and anemia caused by a variety ofconditions, including but not limited to end-stage renal disease(dialysis patients), chronic renal failure in pre-dialysis,zidovudine-treated HIV patients, cancer patients on chemotherapy, andpremature infants; pre-surgery in anemic patients undergoing electivenon-cardiac, non-vascular surgery to reduce the need for bloodtransfusions; aplastic and other refractory anemias, refractory anemiain Inflammatory Bowel Disease, and transfusion avoidance in electiveorthopedic surgery chemoprotection; treating, preventing, and/ordiagnosing inflammatory disorders, myelocytic leukemia, primaryneutropenias (e.g., Kostmann syndrome), secondary neutropenia,prevention of neutropenia, prevention and treatment of neutropenia inHIV-infected patients, prevention and treatment of neutropeniaassociated with chemotherapy, infections associated with neutropenias,myelopysplasia, and autoimmune disorders, mobilization of hematopoieticprogenitor cells, bone marrow transplant, acute myelogeneous leukemia,non-Hodgkin's lymphoma, acute lymphoblastic leukemia, Hodgkin's disease,accelerated myeloid recovery, and glycogen storage disease.

Example 25 Construct ID 2053, IFNb-HSA, Generation

Construct ID 2053, pEE12.1:IFNb.HSA, comprises DNA encoding an IFNbalbumin fusion protein which has the full-length IFNb protein includingthe native IFNb leader sequence fused to the amino-terminus of themature form of HSA in the NSO expression vector pEE12.1.

Cloning of IFNb cDNA

The polynucleotide encoding IFNb was PCR amplified using primers IFNb-1and IFNb-2, described below, cut with Bam HI/Cla I, and ligated into BamHI/Cla I cut pC4:HSA, resulting in construct 2011. The Eco RI/Eco RIfragment from Construct ID #2011 was subcloned into the Eco RI site ofpEE12.1 generating construct ID #2053 which which comprises DNA encodingan albumin fusion protein containing the leader sequence and the matureform of IFNb, followed by the mature HSA protein.

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the full-length of IFNb, IFNb-1 and IFNb-2, weresynthesized:

IFNb-1: (SEQ ID NO: 817)5′-GCGCGGATCCGAATTCCGCCGCCATGACCAACAAGTGTCTCCTCCAAATTGCTCTCCTGTTGTGCTTCTCCACTACAGCTCTTTCCATGAGCTACAA CTTGCTTGG-3′ IFNb-2:(SEQ ID NO: 818) 5′-GCGCGCATCGATGAGCAACCTCACTCTTGTGTGCATCGTTTCGGAGGTAACCTGT-3′

The IFNb-1 primer incorporates a Bam HI cloning site (shown underlined),an Eco RI cloning site, and a Kozak sequence (shown in italics),followed by 80 nucleotides encoding the first 27 amino acids of thefull-length form of IFNb. In IFNb-2, the Cla I site (shown underlined)and the DNA following it are the reverse complement of DNA encoding thefirst 10 amino acids of the mature HSA protein (SEQ ID NO:1038) and thelast 18 nucleotides are the reverse complement of DNA encoding the last6 amino acid residues of IFNb (see Example 2). A PCR amplimer wasgenerated using these primers, purified, digested with Bam HI and Cla Irestriction enzymes, and cloned into the Bam HI and Cla I sites of thepC4:HSA vector. After the sequence was confirmed, an Eco RI fragmentcontaining the IFNb albumin fusion protein expression cassette wassubcloned into Eco RI digested pEE12.1.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected IFNb sequence (see below).

IFNb albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of IFNb, i.e., Met-22 to Asn-187. In oneembodiment of the invention, IFNb albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature IFNb albuminfusion protein is secreted directly into the culture medium. IFNbalbumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, IFNb albumin fusion proteins of theinvention comprise the native IFNb. In further preferred embodiments,the IFNb albumin fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Expression and Purification of Construct ID 2053. Expression in MurineMyeloma NS0 Cell-Lines.

Construct ID #2053, pEE12.1:IFNb-HSA, was electroporated into NSO cellsby methods known in the art (see Example 6).

Purification from NS0 Cell Supernatant.

Purification of IFNb-HSA from NS0 cell supernatant may follow themethods described in Example 10 which involve Q-Sepharose anion exchangechromatography at pH 7.4 using a NaCl gradient from 0 to 1 M in 20 mMTris-HCl, followed by Poros PI 50 anion exchange chromatography at pH6.5 with a sodium citrate gradient from 5 to 40 mM, and diafiltratingfor 6 DV into 10 mM citrate, pH 6.5 and 140 mM NaCl, the final buffercomposition. N-terminal sequencing should yield the sequence MSYNLLwhich is the amino terminus of the mature form of IFNb. The protein hasan approximate MW of 88.5 kDa.

For larger scale purification, e.g., 50 L of NS0 cell supernatant can beconcentrated into ˜8 to 10 L. The concentrated sample can then be passedover the Q-Sepharose anion exchange column (10×19 cm, 1.5 L) at pH 7.5using a step elution consisting of 50 mM NaOAc, pH 6.0 and 150 mM NaCl.The eluted sample can then be virally inactivated with 0.75% Triton-X100 for 60 min at room temperature. SDR-Reverse Phase chromatography (10cm×10 cm, 0.8 L) can then be employed at pH 6.0 with 50 mM NaOAc and 150mM NaCl, or alternatively, the sample can be passed over an SP-sepharosecolumn at pH 4.8 using a step elution of 50 mM NaOAc, pH 6.0, and 150 mMNaCl. DV 50 filtration would follow to remove any viral content.Phenyl-650M chromatography (20 cm×12 cm, 3.8 L) at pH 6.0 using a stepelution consisting of 350 mM (NH₄)₂SO₄ and 50 mM NaOAc, or alternativelyconsisting of 50 mM NaOAc pH 6.0, can follow. Diafiltration for 6-8 DVwill allow for buffer exchange into the desired final formulation bufferof either 10 mM Na₂HPO₄+58 mM sucrose+120 mM NaCl, pH 7.2 or 10 mMcitrate, pH 6.5, and 140 mM NaCl or 25 mM Na₂HPO₄, 100 mM NaCl, pH 7.2.

The Activity of IFNb can be Assayed Using an In Vitro ISRE-SEAP Assay.

All type I Interferon proteins signal through a common receptor complexand a similar Jak/STAT signaling pathway that culminates in theactivation of Interferon, “IFN”, responsive genes through the InterferonSequence Responsive Element, “ISRE”. A convenient assay for type I IFNactivity is a promoter-reporter based assay system that containsmultiple copies of the ISRE element fused to a downstream reporter gene.A stable HEK293 cell-line can be generated and contains a stablyintegrated copy of an ISRE-SEAP reporter gene that is extremelysensitive to type I IFNs and displays linearity over 5 logs ofconcentration.

Method of Screening of IFNb-HSA NS0 Stable Clones.

Construct 2053 was electroporated into NS0 cells as described in Example6. The NS0 cells transfected with construct ID #2053 were screened foractivity by testing conditioned growth media in the ISRE-SEAP assay. TheISRE-SEAP/293F reporter cells were plated at 3×10⁴ cell/well in 96-well,poly-D-lysine coated, plates, one day prior to treatment. Reporter cellswere treated with various dilutions (including but not limited to 1:500and 1:5000) of conditioned supernatant or purified preparations of IFNbalbumin fusion protein encoded by construct ID 2053 or rhIFNb as acontrol. The reporter cells were then incubated for 24 hours prior toremoving 40 □L for use in the SEAP Reporter Gene Chemiluminescent Assay(Roche catalog #1779842). Recombinant human Interferon beta, “rhIFNb”(Biogen), was used as a positive control.

Result

The purified preparation of NS0 expressed IFNb-HSA had a greater EC50 of9.3×10⁻⁹ g/mL than rhIFNb (Biogen) which had an EC50 of 1.8×10⁻¹⁰ g/mL(see FIG. 13).

In Vivo Induction of OAS by an Interferon. Method

The OAS enzyme, 2′-5′-OligoAdenylate Synthetase, is activated at thetranscriptional level by interferon in response to antiviral infection.The effect of interferon constructs can be measured by obtaining bloodsamples from treated monkeys and analyzing these samples fortranscriptional activation of two OAS mRNA, p41 and p69. A volume of 0.5mL of whole blood can be obtained from 4 animals per group at 7different time points, day 0, day 1, day 2, day 4, day 8, day 10, andday 14 per animal. The various groups may include injection of vehiclecontrol, intravenous and/or subcutaneous injection of either 30 □g/kgand/or 300 □g/kg IFN albumin fusion protein on day 1, and subcutaneousinjection of 40 □g/kg of Interferon alpha (Schering-Plough) as apositive control on days 1, 3, and 5. The levels of the p41 and the p69mRNA transcripts can be determined by real-time quantitative PCR(Taqman) using probes specific for p41-OAS and p69-OAS. OAS mRNA levelscan be quantitated relative to 18S ribosomal RNA endogenous control.

In Vivo Induction of OAS by Interferon Beta Albumin Fusion Encoded byConstruct ID 2053. Method

The activity of the HSA-IFNb fusion protein encoded by construct 2053can be assayed in the in vivo OAS assay as previously described aboveunder subsection heading, “In vivo induction of OAS by an Interferon”.

Example 26 Indications for IFNb Albumin Fusion Proteins

IFN beta albumin fusion proteins (including, but not limited to, thoseencoded by construct 2053) can be used to treat, prevent, ameliorateand/or detect multiple sclerosis. Other indications include, but are notlimited to, melanoma, solid tumors, cancer, bacterial infections,chemoprotection, thrombocytopenia, HIV infections, prostate cancer,cancer, hematological malignancies, hematological disorders,preleukemia, glioma, hepatitis B, hepatitis C, human papillomavirus,pulmonary fibrosis, age-related macular degeneration, brain cancer,glioblastoma multiforme, liver cancer, malignant melanoma, colorectalcancer, Crohn's disease, neurological disorders, non-small cell lungcancer, rheumatoid arthritis, and ulcerative colitis.

Example 27 Construct ID 1941, HSA-PTH84, Generation

Construct ID 1941, pC4.HSA.PTH84, encodes for an HSA-PTH84 fusionprotein which comprises the full-length of HSA including the native HSAleader sequence, fused to the mature form of the human parathyroidhormone, “PTH84” Ser-1 to Gln-84, cloned into the mammalian expressionvector pC4.

Cloning of PTH84 cDNA for Construct 1941

The DNA encoding PTH84 was amplified with primers PTH84-1 and PTH84-2,described below, cut with Bsu 36I/Not I, and ligated into Bsu 36I/Not Icut pC4:HSA. Construct ID #1941 encodes an albumin fusion proteincontaining the full-length form of HSA that includes the native HSAleader sequence, followed by the mature PTH84 protein.

Two primers suitable for PCR amplification of the polynucleotideencoding the mature form of PTH84, PTH84-1 and PTH84-2, weresynthesized.

PTH84-1: (SEQ ID NO: 787)5′-GAGCGCGCCTTAGGCTCTGTGAGTGAAATACAGCTTATGCATAAC- 3′ PTH84-2: (SEQ IDNO: 788) 5′-CGGTGCGCGGCCGCTTACTGGGATTTAGCTTTAGTTAATACATTCAC ATC-3′

PTH84-1 incorporates a Bsu 36I cloning site (shown in italics) followedby the nucleic acid sequence encoding amino acid residues Ala-Leu-Glycorresponding to the end of the mature form of HSA (the last Leu isabsent) in conjunction with amino acid residues Ser-1 to Asn-10 of themature form of PTH84. In PTH84-2, the Not I site is shown in italics andthe nucleic acid sequence that follows corresponds to the reversecomplement of DNA encoding the last 11 amino acids of the mature PTH84protein. Using these two primers, the PTH84 protein was PCR amplified.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedHSA sequence (see below).

PTH84 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of PTH84, i.e., Ser-1 to Gln-84. In oneembodiment of the invention, PTH84 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature PTH84 albuminfusion protein is secreted directly into the culture medium. PTH84albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, PTH84 albumin fusion proteins of theinvention comprise the native PTH84. In further preferred embodiments,the PTH84 albumin fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Expression and Purification of Construct ID 1941. Expression in 293TCells.

Construct 1941 was transfected into 293T cells by methods known in theart (e.g., lipofectamine transfection) and selected with 100 nMmethotrexate (see Example 6). Expression levels were examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from 293T Cell Supernatant.

The 293T cell supernatant containing the secreted HSA-PTH84 fusionprotein expressed from construct ID #1941 in 293T cells was purified asdescribed in Example 7. Specifically, initial capture was performed withan anionic HQ-50 resin at pH 7.2 using a sodium phosphate buffer (25 mMNa₂HPO₄ pH 7.2) and 16 column volumes of a salt gradient elution of 0 to0.5 M NaCl, followed by Hydrophobic Interaction Chromatography, “HIC”,with the Phenyl 650 M resin (from Tosohaas) using 36 column volumes of asalt gradient elution of 2.75 to 0 M NaCl at pH 7.2 where the sample hada final conductivity of 180 mS. The sample was concentrated using the HQPoros 50 resin and a salt step elution of 0.15 M NaCl increments. Thefinal buffer composition consisted of 25 mM Na₂HPO₄+150 mM NaCl pH 7.2.N-terminal sequencing generated the amino-terminus sequence (i.e.,DAHKS, SEQ ID NO:2143) of the mature form of HSA. A protein ofapproximate MW of 78 kDa was obtained. A final yield of 0.78 mg proteinper litre of 293T cell supernatant was obtained.

In Vitro Induction of Cyclic AMP in SaOS2 Cells. Method

The biological activity of a PTH84 albumin fusion protein can bemeasured in an in vitro assay in which SaOS-2, an osteosarcomacell-line, is used. PTH activates adenylate cyclase thereby increasingintracellular cyclic AMP levels.

Induction of cAMP in SaOS-2 Cells:

The SaOS-2 cells are subcultured at a density of 8.0×10⁴ cells/well 24hours prior to the start of the experiment. On the day of theexperiment, the cells are serum starved for 2 hours and then treated for10 minutes with positive controls (e.g., forskolin at 5 mg/mL),recombinant PTH, or the PTH albumin fusion proteins. Followingtreatment, the cells are then rinsed and the intracellular cyclic AMP isextracted with cold ethanol. The ethanol extracts can be lyophilized andstored at −80° C. for further use. The amount of cyclic AMP present inthe samples is quantitated by ELISA as per the manufacturer's protocol(Amersham Life Sciences, Inc.).

In Vitro Induction of Cyclic AMP in SaOS2 Cells by the Albumin FusionProtein Encoded by Construct 1941. Method

The in vitro assay to measure the induction of cyclic AMP in SaOS2 cellsby the PTH albumin fusion protein encoded by construct 1941 can becarried out as previously described above.

In Vivo: Induced Release of Calcium in TPTX Animals. Methods

PTH activity is tested by monitoring the PTH albumin fusion proteinsability to reduce the demineralization of bone followingThyroParaThyroidectomy, “TPTX”, administration of a low calcium diet,and parathyroid hormone treatment.

The animals display a variability in pharmacological response assuggested by Votta, et al., 1997, J. Bone and Mineral Res., 12:1396-1406; Millest, et al., 1997, Bone, 20: 465-471; and Iwata, et al.,1997, Arthritis and Rheumatism, 40: 499-509. Therefore, between 5 and 8thyroparathyroidectomized animals (purchased from an outside vendor) pergroup are used. The animals receive replacement injections of thyroxineevery other day. Each experiment will include several groups: (1)placebo and parathyroid hormone (PTH 1-34) injected groups whichcorrespond to the negative and positive controls, respectively; (2-5)PTH albumin fusion proteins, at various concentrations ranging from 0.1to 12 μg/kg, injected intravenously, intraperitoneally, subcutaneously,and intramuscular, either before, during, or after parathyroid hormonetreatment; (6) for some experiments, a cysteine protease inhibitor istested.

Under isofluorane anesthesia, the left femoral vein and either the leftfemoral artery or carotid artery is cannulated with PE-10 tubing fusedto PE-50 polyethylene tubing filled with heparinized saline. Thecatheters are tunneled subcutaneously, exteriorized at the nape andsecured to the skin. The animals are allowed to recover forapproximately 18 hours prior to being used for experimentation duringwhich time they are given a calcium free diet. During the course of theexperiment, 3 blood samples (200 mL each) are taken via the carotid orfemoral catheter following 2, 4, and 6 hours of infusion. Longer timepoints, e.g., 18 hours, may also be desirable.

A dose relationship between human PTH 1-34, the positive control, andthe appearance of ionized calcium levels in whole blood was established(data not shown).

The Activity of the Albumin Fusion Protein Encoded by Construct 1941 canbe Assayed Using TPTX Animals.

The activity of the PTH albumin fusion protein encoded by construct 1941can be measured using TPTX animals and the in vivo assay described aboveunder the heading, “In vivo: Induced release of calcium in TPTXanimals”.

An In Vivo Ovariectomized Female Rat Model. Methods

PTH activity is tested by monitoring the ability to induce boneformation in ovariectomized female Lewis or Sprague Dawley rats.

Surgery is performed on female Lewis or Sprague Dawley rats 8-9 weeks ofage and experiments are not initiated until 7 to 10 days after thesurgery. Samples from blood, urine, and left tibia are obtained weeklyfrom 9 to 12 animals per group. The various groups can include a shamcontrol injected with saline everyday for four weeks, ovariectomizedrats injected with saline everyday for four weeks, and ovariectomizedrats injected with rat PTH peptide 1-34 at 10 □g/kg subcutaneously fivetimes per week. Following the fourth and final week of tissuecollection, the tibias are sent to Skeletech for bone densitometryanalysis.

The parameters tested are body weight, bone densitometry on left tibiain 70% ethanol, serum pyridinoline from blood, and urinedeoxypyridinoline and alpha helical protein. Urine samples are taken inthe morning. Blood is obtained from bleeding the heart and the serum issaved for ELISA analysis. Bone densitometry is conducted on the proximaltibia. The left femur can be cut with bone shears just above the knee.The paw can also be removed by cutting the distal tibia. The skin isslit laterally to allow in ethanol and the remainder of the limb is putin a 50 cc tube filled with 70% ethanol. The tube is stored at roomtemperature until shipped. The rat tibial specimens are allowed to thawto room temperature the day of the testing. Excised rat tibiae aresubjected to bone mineral density determinations using peripheralquantitative computed tomography (pQCT, XCT-RM, Norland/Stratec). Thescan is performed at a proximal tibia site (12% of the total length awayfrom the proximal end). One 0.5 mm slice is taken. Scans are analyzed asa whole (total bone) or using a threshold delineation of external andinternal boundaries (cortical bone) or an area that is 45% of the totalbone tissue by peeling from the outer edge (cancellous bone). Bonemineral density, area and content are then determined by systemsoftware. The differences between sham and ovariectomized animals, ateach different time point, are determined by two-tailed t-test using SASstatistical software (SAS Institute, Cory, N.C.). The student t test isused for statistical comparison of means. P values of less than 0.05 areconsidered statistically significant.

The Activity of the Albumin Fusion Protein Encoded by Construct 1941 canbe Assayed Using the In Vivo Ovariectomized Female Rat Model.

The activity of the PTH albumin fusion protein encoded by construct 1941can be measured using the in vivo assay described above under theheading, “An in vivo ovariectomized female rat model”.

Example 28 Construct ID 1949, PTH84-HSA, Generation

Construct ID 1949, pC4.PTH84.S1-Q84.HSA, encodes a PTH84-HSA fusionprotein which comprises the MPIF leader sequence, followed by the matureform of PTH84, i.e., Ser-1 to Gln-84, fused to the amino-terminus of themature form of HSA cloned into the mammalian expression vector pC4.

Cloning of PTH84 cDNA for Construct 1949

The DNA encoding PTH84 was amplified with primers PTH84-3 and PTH84-4,described below, cut with Bam HI/SpeI, and ligated into Bam HI/XbaI cutpC4:HSA. Construct ID #1949 encodes an albumin fusion protein comprisingthe mature PTH84 protein followed by the mature form of HSA.

Two primers suitable for PCR amplification of the polynucleotideencoding the mature form of PTH84, PTH84-3 and PTH84-4, weresynthesized.

PTH84-3: (SEQ ID NO: 793)5′-GAGCGCGGATCCGCCATCATGAAGGTCTCCGTGGCTGCCCTCTCCTGCCTCATGCTTGTTACTGCCCTTGGATCTCAGGCC TCTGTGAGTGAAATAC AGCTTATGC-3′PTH84-4: (SEQ ID NO: 794) 5′-GTCGTCACTAGTCTGGGATTTAGCTTTAGTTAATACATTCAC- 3′

PTH84-3 incorporates a Bam HI cloning site (shown in italics) followedby a nucleic acid sequence that encodes the MPIF signal peptide (shownunderlined) and amino acid residues Ser-1 to Met-8 (shown in bold) ofthe mature form of PTH84. In PTH84-4, the SpeI site is shown in italicsand the nucleic acid sequence that follows corresponds to the reversecomplement of DNA encoding the last 10 amino acids of the mature PTH84protein (shown in bold). Using these two primers, the PTH84 protein wasPCR amplified. The PCR amplimer was purified, digested with Bam HI andSpeI and ligated into Bam HI/XbaI cut pC4:HSA.

There are two additional amino acid residues, i.e., Thr and Ser, betweenPTH84 and HSA as a result of the introduction of the SpeI cloning siteinto the PTH84-4 primer.

Further analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing confirmed the presence of the expectedPTH84 sequence (see below).

PTH84 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of PTH84, i.e., Ser-1 to Gln-84. In oneembodiment of the invention, PTH84 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature PTH84 albuminfusion protein is secreted directly into the culture medium. PTH84albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, PTH84 albumin fusion proteins of theinvention comprise the native PTH84. In further preferred embodiments,the PTH84 albumin fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Expression and Purification of Construct ID 1949. Expression in 293TCells.

Construct 1949 was transfected into 293T cells by methods known in theart (e.g., lipofectamine transfection) and selected with 100 nMmethotrexate (see Example 6). Expression levels were examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from 293T Cell Supernatant.

The 293T cell supernatant containing the secreted PTH84-HSA fusionprotein expressed from construct ID #1949 in 293T cells was purified asdescribed in Example 7. Specifically, initial capture was performed withan anionic HQ-50 resin at pH 7.2 using a sodium phosphate buffer (25 mMNa₂HPO₄ pH 7.2) and 16 column volumes of a salt gradient elution of 0 to0.5 M NaCl, followed by Hydrophobic Interaction Chromatography, “HIC”,with the Phenyl 650 M resin (from Tosohaas) using 36 column volumes of asalt gradient elution of 2.75 to 0 M NaCl at pH 7.2 where the sample hada final conductivity of 180 mS. The sample was concentrated using the HQPoros 50 resin and a salt step elution of 0.15 M NaCl increments. Thefinal buffer composition consisted of 25 mM Na₂HPO₄+150 mM NaCl pH 7.2.N-terminal sequencing generated the amino-terminus sequence (i.e.,SVSEI, SEQ ID NO:2145) of the mature form of PTH84. A protein ofapproximate MW of 78 kDa was obtained. A final yield of 0.32 mg proteinper litre of 293T cell supernatant was obtained.

In Vitro Induction of Cyclic AMP in SaOS2 Cells by the Albumin FusionProtein Encoded by Construct 1949. Result

A purified HSA-PTH84 albumin fusion protein derived from 293T cellsexpressing construct 1949 was tested in the in vitro assay described inExample 27 under subsection heading, “In vitro induction of cyclic AMPin SaOS2 cells”. HSA-PTH84 induced an increase in intracellular cyclicAMP levels.

The Activity of the Albumin Fusion Protein Encoded by Construct 1949 canbe Assayed Using TPTX Animals.

The activity of the PTH albumin fusion protein encoded by construct 1949can be measured using TPTX animals and the in vivo assay described inExample 27 under the subsection heading, “In vivo: Induced release ofcalcium in TPTX animals”.

The Activity of the Albumin Fusion Protein Encoded by Construct 1949 canbe Assayed Using the In Vivo Ovariectomized Female Rat Model.

The activity of the PTH albumin fusion protein encoded by construct 1949can be measured using the in vivo assay described in Example 27 underthe subsection heading, “An in vivo ovariectomized female rat model”.

Example 29 Construct ID 2021, PTH84-HSA, Generation

Construct ID 2021, pC4.PTH84.S1-Q84.HSA, encodes for an PTH84-HSA fusionprotein which comprises the native HSA leader, followed by the matureform of PTH84, i.e., Ser-1 to Gln-84, fused to the amino-terminus of themature form of HSA cloned into the mammalian expression vector pC4.

Cloning of PTH84 cDNA for Construct 2021

The DNA encoding PTH84 was amplified with primers PTH84-5 and PTH84-6,described below, cut with Xho I/Cla I, and ligated into Xho I/Cla I cutpC4:HSA. Construct ID #2021 encodes an albumin fusion protein containingthe mature PTH84 protein followed by the mature form of HSA (see Example5).

Two primers suitable for PCR amplification of the polynucleotideencoding the mature form of PTH84, PTH84-5 and PTH84-6, weresynthesized.

PTH84-5: (SEQ ID NO: 823) 5′-CCGCCG CTCGAGGGGTGTGTTTCGTCGATCTGTGAGTGAAATACAGC TTATGCATAAC-3′ PTH84-6: (SEQ ID NO: 824)5′-AGTCCCATCGATGAGCAACCTCACTCTTGTGTGCATC CTGGGATTTAGCTTTAGTTAATACATTCACATC-3′

PTH84-5 incorporates a Xho I cloning site (shown in italics). The Xho Isite combined with the nucleic acid sequence that follows (shownunderlined) encodes for the last four amino acid residues of thechimeric signal peptide of HSA. The nucleic acid sequence in boldencodes for amino acid residues Ser-1 to Asn-10 of the mature form ofPTH84. In PTH84-6, the Cla I site is shown in italics and the nucleicacid sequence that follows (shown underlined) corresponds to the reversecomplement of DNA encoding the first 10 amino acids of the mature formof HSA. The nucleic acid sequence highlighted in bold in PTH84-6corresponds to the reverse complement of DNA encoding the last 11 aminoacids of the mature form of PTH84. Using these two primers, the PTH84protein was PCR amplified. The PCR amplimer was purified, digested withXho I and Cla I and ligated into Xho I/Cla I cut pC4:HSA.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected PTH84 sequence (see below).

PTH84 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of PTH84, i.e., Ser-1 to Gln-84. In oneembodiment of the invention, PTH84 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature PTH84 albuminfusion protein is secreted directly into the culture medium. PTH84albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, PTH84 albumin fusion proteins of theinvention comprise the native PTH84. In further preferred embodiments,the PTH84 albumin fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Expression and Purification of Construct ID 2021. Expression in 293TCells.

Construct 2021 can be transfected into 293T cells by methods known inthe art (e.g., lipofectamine transfection) and selected with 100 nMmethotrexate (see Example 6). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from 293T Cell Supernatant.

The 293T cell supernatant containing the secreted PTH84-HSA fusionprotein expressed from construct ID #2021 in 293T cells can be purifiedas described in Example 7. Specifically, initial capture can beperformed with an anionic HQ-50 resin at pH 7.2 using a sodium phosphatebuffer (25 mM Na₂HPO₄ pH 7.2) and 16 column volumes of a salt gradientelution of 0 to 0.5 M NaCl, followed by Hydrophobic InteractionChromatography, “HIC”, with the Phenyl 650 M resin (from Tosohaas) using36 column volumes of a salt gradient elution of 2.75 to 0 M NaCl at pH7.2 where the sample has a final conductivity of 180 mS. The sample canbe concentrated using the HQ Poros 50 resin and a salt step elution of0.15 M NaCl increments. The final buffer composition may consist of 25mM Na₂HPO₄+150 mM NaCl pH 7.2. N-terminal sequencing should generate theamino-terminus sequence (i.e., SVSEI) of the mature form of PTH84. Aprotein of approximate MW of 78 kDa should be obtained.

In Vitro Induction of Cyclic AMP in SaOS2 Cells by the Albumin FusionProtein Encoded by Construct 2021.

HSA-PTH84 albumin fusion protein derived from 293T cells expressingconstruct 2021 can be tested in the in vitro assay described in Example27 under subsection heading, “In vitro induction of cyclic AMP in SaOS2cells”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2021 canbe Assayed Using TPTX Animals.

The activity of the PTH albumin fusion protein encoded by construct 2021can be measured using TPTX animals and the in vivo assay described inExample 27 under the subsection heading, “In vivo: Induced release ofcalcium in TPTX animals”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2021 canbe Assayed Using the In Vivo Ovariectomized Female Rat Model.

The activity of the PTH albumin fusion protein encoded by construct 2021can be measured using the in vivo assay described in Example 27 underthe subsection heading, “An in vivo ovariectomized female rat model”.

Example 30 Indications for PTH84 Albumin Fusion Proteins

Results from in vitro and in vivo assays described above indicate thatPTH84 albumin fusion proteins are useful for the treatment, prevention,and/or diagnosis of osteoporosis, malignant hypercalcaemia, and Paget'sdisease.

Example 31 Construct ID 2249, IFNa2-HSA, Generation

Construct ID 2249, pSAC35:IFNa2.HSA, comprises DNA encoding an IFNa2albumin fusion protein which has the HSA chimeric leader sequence,followed by the mature form of IFNa2 protein, i.e., C1-E165, fused tothe amino-terminus of the mature form of HSA in the yeast S. cerevisiaeexpression vector pSAC35.

Cloning of IFNa2 cDNA

The polynucleotide encoding IFNa2 was PCR amplified using primersIFNa2-1 and IFNa2-2, described below. The PCR amplimer was cut with SalI/Cla I, and ligated into Xho I/Cla I cut pScCHSA. Construct ID #2249encodes an albumin fusion protein containing the chimeric leadersequence of HSA, the mature form of IFNa2, followed by the mature HSAprotein.

Two oligonucleotides suitable for PCR amplification of thepolynucleotide encoding the mature form of IFNa2, IFNa2-1 and IFNa2-2,were synthesized:

IFNa2-1: (SEQ ID NO: 887)5′-CGCGCGCGTCGACAAAAGATGTGATCTGCCTCAAACCCACA-3′ IFNa2-2: (SEQ ID NO:888) 5′-GCGCGCATCGATGAGCAACCTCACTCTTGTGTGCATCTTCCTTACTT CTTAAACTTTCT-3′

The IFNa2-1 primer incorporates a Sal I cloning site (shown underlined),nucleotides encoding the last three amino acid residues of the chimericHSA leader sequence, as well as 22 nucleotides (shown in bold) encodingthe first 7 amino acid residues of the mature form of IFNa2. In IFNa2-2,the Cla I site (shown underlined) and the DNA following it are thereverse complement of DNA encoding the first 10 amino acids of themature HSA protein and the last 22 nucleotides (shown in bold) are thereverse complement of DNA encoding the last 7 amino acid residues ofIFNa2 (see Example 2). A PCR amplimer of IFNa2-HSA was generated usingthese primers, purified, digested with Sal I and Cla I restrictionenzymes, and cloned into the Xho I and Cla I sites of the pScCHSAvector. After the sequence was confirmed, the expression cassetteencoding this IFNa2 albumin fusion protein was subcloned into Not Idigested pSAC35.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected IFNa2 sequence (see below).

Other IFNa2 albumin fusion proteins using different leader sequenceshave been constructed by methods known in the art (see Example 2).Examples of the various leader sequences include, but are not limitedto, invertase “INV” (constructs 2343 and 2410) and mating alpha factor“MAF” (construct 2366). These IFNa2 albumin fusion proteins can besubcloned into mammalian expression vectors such as pC4 (constructs2382) and pEE12.1 as described previously (see Example 5). IFNa2 albuminfusion proteins with the therapeutic portion fused C-terminus to HSA canalso be constructed (construct 2381).

IFNa2 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of IFNa2, i.e., Cys-1 to Glu-165. In oneembodiment of the invention, IFNa2 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature IFNa2 albuminfusion protein is secreted directly into the culture medium. IFNa2albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, IFNa2 albumin fusion proteins of theinvention comprise the native IFNa2. In further preferred embodiments,the IFNa2 albumin fusion proteins of the invention further comprise anN-terminal methionine residue. Polynucleotides encoding thesepolypeptides, including fragments and/or variants, are also encompassedby the invention.

Expression and Purification of Construct ID 2249.

Expression in Yeast S. cerevisiae.

Transformation of construct 2249 into yeast S. cerevisiae strain BXP10was carried out by methods known in the art (see Example 3). Cells canbe collected at stationary phase after 72 hours of growth. Supernatantsare collected by clarifying cells at 3000 g for 10 min. Expressionlevels are examined by immunoblot detection with anti-HSA serum (KentLaboratories) or as the primary antibody. The IFNa2 albumin fusionprotein of approximate molecular weight of 88.5 kDa can be obtained.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing IFNa2 albumin fusion protein expressedfrom construct ID #2249 in yeast S. cerevisiae cells can be purifiedeither small scale over a Dyax peptide affinity column (see Example 4)or large scale by following 5 steps: diafiltration, anion exchangechromatography using DEAE-Sepharose Fast Flow column, hydrophobicinteraction chromatography (HIC) using Butyl 650S column, cationexchange chromatography using an SP-Sepharose Fast Flow column or aBlue-Sepharose chromatography, and high performance chromatography usingQ-sepharose high performance column chromatography (see Example 4). TheIFNa2 albumin fusion protein may elute from the DEAE-Sepharose Fast Flowcolumn with 100-250 mM NaCl, from the SP-Sepharose Fast Flow column with150-250 mM NaCl, and from the Q-Sepharose High Performance column at5-7.5 mS/cm. N-terminal sequencing should yield the sequence CDLPQ (SEQID NO:2146) which corresponds to the mature form of IFNa2.

The Activity of IFNa2 can be Assayed Using an In Vitro ISRE-SEAP Assay.Method

The IFNa2 albumin fusion protein encoded by construct ID #2249 can betested for activity in the ISRE-SEAP assay as previously described inExample 25. Briefly, conditioned yeast supernatants were tested at a1:1000 dilution for their ability to direct ISRE signal transduction onthe ISRE-SEAP/293F reporter cell-line. The ISRE-SEAP/293F reporter cellswere plated at 3×10⁴ cell/well in 96-well, poly-D-lysine coated, plates,one day prior to treatment. The reporter cells were then incubated for18 or 24 hours prior to removing 40 μL for use in the SEAP Reporter GeneChemiluminescent Assay (Roche catalog #1779842). Recombinant humanInterferon beta, “rhIFNb” (Biogen), was used as a positive control.

Result

The purified preparation of IFNa2-HSA demonstrated a relatively linearincrease in the ISRE-SEAP assay over concentrations ranging from 10⁻¹ to10¹ ng/mL (see FIG. 15) or 10⁻¹⁰ to 10⁻⁸ ng/mL (see FIG. 16).

In Vivo Induction of OAS by Interferon Alpha Fusion Encoded by ConstructID 2249. Method

The OAS enzyme, 2′-5′-OligoAdenylate Synthetase, is activated at thetranscriptional level by interferon in response to antiviral infection.The effect of interferon constructs can be measured by obtaining bloodsamples from treated monkeys and analyzing these samples fortranscriptional activation of two OAS mRNA, p41 and p69. A volume of 0.5mL of whole blood was obtained from 4 animals per group at 7 differenttime points, day 0, day 1, day 2, day 4, day 8, day 10, and day 14 peranimal. The various groups include vehicle control, intravenousinjection of 30 μg/kg HSA-IFN on day 1, subcutaneous injection of 30μg/kg of HSA-IFN on day 1, subcutaneous injection of 300 μg/kg ofHSA-IFN on day 1, and subcutaneous injection of 40 μg/kg of Interferonalpha (Schering-Plough) as a positive control on days 1, 3, and 5. Thelevels of the p41 and the p69 mRNA transcripts were determined byreal-time quantitative PCR (Taqman) using probes specific for p41-OASand p69-OAS. OAS mRNA levels were quantitated relative to 18S ribosomalRNA endogenous control. The albumin fusion encoded by construct 2249 canbe subjected to similar experimentation.

Results

A significant increase in mRNA transcript levels for both p41 and p69OAS was observed in HSA-interferon treated monkeys in contrast to IFNatreated monkeys (see FIG. 17 for p41 data). The effect lasted nearly 10days.

Example 32 Indications for IFNa2 Albumin Fusion Proteins

IFN alpha albumin fusion protein (including, but not limited to, thoseencoded by constructs 2249, 2343, 2410, 2366, 2382, and 2381) can beused to treat, prevent, ameliorate, and/or detect multiple sclerosis.Other indications include, but are not limited to, Hepatitis C, oncologyuses, cancer, hepatitis, human papilloma virus, fibromyalgia, Sjogren'ssyndrome, hairy cell leukemia, chronic myelogeonus leukemia,AIDS-related Kaposi's sarcoma, chronic hepatitis B, malignant melanoma,non-Hodgkin's lymphoma, external condylomata acuminata, HIV infection,small cell lung cancer, hematological malignancies, herpes simplex virusinfections, multiple sclerosis, viral hemorrhagic fevers, solid tumors,renal cancer, bone marrow disorders, bone disorders, bladder cancer,gastric cancer, hepatitis D, multiple myeloma, type I diabetes mellitus,viral infections, cutaneous T-cell lymphoma, cervical dysplasia, chronicfatigue syndrome, and renal cancer.

Preferably, the IFNα-albumin fusion protein or IFN hybrid fusion proteinis administered in combination with a CCR5 antagonist, further inassociation with at least one of ribavirin, IL-2, IL-12, pentafusidealone or in combination with an anti-HIV drug therapy, e.g., HAART, forpreparation of a medicament for the treatment of HIV-1 infections, HCV,or HIV-1 and HCV co-infections in treatment-naïve as well astreatment-experienced adult and pediatric patients.

Example 33 Construct ID 2250, HSA-Insulin (GYG), Generation

Construct ID 2250, pSAC35.HSA.INSULIN(GYG).F1-N62, encodes for anHSA-INSULIN (GYG) fusion protein which comprises full length HSA,including the native HSA leader sequence, fused to the amino-terminus ofthe synthetic single-chain long-acting insulin analog (INSULIN (GY³²G))with a Tyr at position 32, cloned into the yeast S. cerevisiaeexpression vector pSAC35.

Cloning of INSULIN (GYG) cDNA for Construct 2250.

The DNA encoding the synthetic single-chain form of INSULIN (GYG) wasPCR generated using four overlapping primers. The sequence correspondingto the C-peptide in the middle region of the proinsulin cDNA wasreplaced by the C-domain of Insulin Growth Factor 1, “IGF-1”(GY³²GSSSRRAPQT, SEQ ID NO:2147), to avoid the need for proinsulinprocessing and to ensure proper folding of the single-chain protein. Thesequence was codon optimized for expression in yeast S. cerevisiae. ThePCR fragment was digested and subcloned into Bsu 361/Asc I digestedpScNHSA. A Not I fragment was then subcloned into the pSAC35 plasmid.Construct ID #2250 encodes for full length HSA, including the native HSAleader sequence, fused to the amino-terminus of the syntheticsingle-chain form of INSULIN (GYG).

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the syntheticsingle-chain form of INSULIN (GYG), INSULIN (GYG)-1 and INSULIN (GYG)-2,were synthesized:

INSULIN (GYG)-1: (SEQ ID NO: 889)5′-GTCAAGCTGCCTTAGGCTTATTCGTTAACCAACACTTGTGTGGTTCTCACTTGGTTGAAGCTTTGTACTTGGTTTGTGGTGAA-3′ INSULIN (GYG)-2: (SEQ ID NO:890) 5′-ATCGCATATGGCGCGCCCTATTAGTTACAGTAGTTTTCCAATTGGTACAAAGAACAAATAGAAGTACAA-3′

INSULIN (GYG)-1 incorporates a Bsu 36I cloning site (shown in italics)and encodes the first 21 amino acids (shown in bold) of the ORF of thesynthetic single-chain form of INSULIN (GYG). In INSULIN (GYG)-2, theitalicized sequence is an Asc I site. In INSULIN (GYG)-2, the boldedsequence is the reverse complement of the last 49 nucleotides encodingamino acid residues Cys-49 to Asn-63 of the synthetic single-chain formof INSULIN (GYG). With these two primers, the synthetic single-chainform of INSULIN (GYG) was PCR amplified. Annealing and extensiontemperatures and times must be empirically determined for each specificprimer pair and template.

The PCR product was purified (for example, using Wizard PCR Preps DNAPurification System (Promega Corp)) and then digested with Bsu36I andAscI. After further purification of the Bsu36I-AscI fragment by gelelectrophoresis, the product was cloned into Bsu36I/AscI digestedpScNHSA. A Not I fragment was further subcloned into pSAC35 to giveconstruct ID #2250.

Further analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing should confirm the presence of theexpected mature HSA sequence (see below).

INSULIN albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the synthetic single-chain analog of INSULIN, i.e., Phe-1to Asn-62; the sequence corresponding to the C-peptide in the middleregion of the proinsulin cDNA was replaced by the C-domain of InsulinGrowth Factor 1, “IGF-1” (GY³²GSSSRRAPQT, SEQ ID NO:2147). In oneembodiment of the invention, INSULIN albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature INSULINalbumin fusion protein is secreted directly into the culture medium.INSULIN albumin fusion proteins of the invention may compriseheterologous signal sequences including, but not limited to, MAF, INV,Ig, Fibulin B, Clusterin, Insulin-Like Growth Factor Binding Protein 4,variant HSA leader sequences including, but not limited to, a chimericHSA/MAF leader sequence, or other heterologous signal sequences known inthe art. In a preferred embodiment, INSULIN albumin fusion proteins ofthe invention comprise the native INSULIN. In further preferredembodiments, the INSULIN albumin fusion proteins of the inventionfurther comprise an N-terminal methionine residue. Polynucleotidesencoding these polypeptides, including fragments and/or variants, arealso encompassed by the invention.

Expression and Purification of Construct ID 2250.

Expression in Yeast S. cerevisiae.

Construct 2250 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted INSULIN (GYG) albuminfusion protein expressed from construct ID #2250 in yeast S. cerevisiaecan be purified as described in Example 4. N-terminal sequencing of thealbumin fusion protein should result in the sequence DARKS (SEQ IDNO:2143) which corresponds to the amino terminus of the mature form ofHSA.

In Vitro [³H]-2-Deoxyglucose Uptake Assay in the Presence of the AlbuminFusion Protein Encoded by Construct 2250. Method

The in vitro assay to measure the glucose uptake in 3T3-L1 adipocytes inthe presence of the INSULIN (GYG) albumin fusion protein encoded byconstruct 2250 was carried out as described below in Example 41. Otherassays known in the art that may be used to test INSULIN (GYG) albuminfusion proteins' include, but are not limited to, L6 Rat MyoblastProliferation Assay via glycogen synthase kinase-3 (GSK-3) and H4IIereporter assays (see Example 48) including the rat Malic Enzyme Promoter(rMEP)-SEAP, Sterol Regulatory Element Binding Protein (SREBP)-SEAP,Fatty Acid Synthetase (FAS)-SEAP, and PhosphoEnolPyruvate CarboxyKinase(PEPCK)-SEAP reporters.

Result

The supernatant derived from transformed yeast S. cerevisiae expressinginsulin albumin fusion encoded by construct 2250 demonstrated glucoseuptake/transport activity in 3T3-L1 adipocytes (see FIG. 18).

In Vitro Pancreatic Cell-Lines Proliferation Assay in the Presence ofthe Albumin Fusion Protein Encoded by Construct 2250. Method

The in vitro assay to measure the differentiation and proliferation ofductal epithelium pancreatic ARIP cell-line into insulin-producing betacells and/or to measure the proliferation of the insulin-producing RIN-Mbeta cell-line in the presence of the INSULIN (GYG) albumin fusionprotein encoded by construct 2250 can be carried out as described belowunder heading: “Example 42: In vitro Assay of [³H]-ThymidineIncorporation into Pancreatic Cell-lines”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2250 canbe Assayed In Vivo Using Diabetic NOD and/or NIDDM Mouse Models.

The activity of the INSULIN (GYG) albumin fusion protein encoded byconstruct 2250 can be measured using NOD and/or NIDDM mouse modelsdescribed below under the headings, “Example 44: Occurrence of Diabetesin NOD Mice”, “Example 45: Histological Examination of NOD Mice”, and“Example 47: In vivo Mouse Model of NIDDM”.

Example 34 Construct ID 2255, Insulin (GYG)-HSA, Generation

Construct ID 2255, pSAC35.INSULIN(GYG).F1-N62.HSA, encodes for anINSULIN (GYG)-HSA fusion protein which comprises the HSA chimeric leadersequence of HSA fused to the amino-terminus of the syntheticsingle-chain long-acting insulin analog (INSULIN (GY³²G)) with a Tyr inposition 32, which is, in turn, fused to the mature form of HSA, clonedinto the yeast S. cerevisiae expression vector pSAC35.

Cloning of INSULIN (GYG) cDNA for Construct 2255.

The DNA encoding the synthetic single-chain form of INSULIN (GYG) wasPCR generated using four overlapping primers. The sequence correspondingto the C-peptide in the middle region of the proinsulin cDNA wasreplaced by the C-domain of Insulin Growth Factor 1, “IGF-1”(GY³²GSSSRRAPQT, SEQ ID NO:2147), to avoid the need for proinsulinprocessing and to ensure proper folding of the single-chain protein. Thesequence was codon optimized for expression in yeast S. cerevisiae. ThePCR fragment was digested with Sal I/Cla I and subcloned into Xho I/ClaI digested pScCHSA. A Not I fragment was then subcloned into the pSAC35plasmid. Construct ID #2255 encodes for the chimeric leader sequence ofHSA fused to the amino-terminus of the synthetic single-chain form ofINSULIN (GYG) followed by the mature form of HSA.

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the syntheticsingle-chain form of INSULIN (GYG), INSULIN (GYG)-3 and INSULIN (GYG)-4,were synthesized:

INSULIN (GYG)-3: (SEQ ID NO: 895)5′-TCCAGGAGCGTCGACAAAAGATTCGTTAACCAACACTTGTGTGGTTCTCACTTGGTTGAAGCTTTGTACTTGGTTTGTGGTGAA-3′ INSULIN (GYG)-4: (SEQ ID NO:896) 5′-AGACTTTAAATCGATGAGCAACCTCACTCTTGTGTGCATCGTTACAGTAGTTTTCCAATTGGTACAAAGAACAAATAGAAGTACAA-3′INSULIN (GYG)-3 incorporates a Sal I cloning site (shown in italics) andthe DNA encoding the first 21 amino acids (shown in bold) of the ORF ofthe synthetic single-chain form of INSULIN(GYG). In INSULIN (GYG)-4, theitalicized sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein. The bolded sequence is thereverse complement of the 46 nucleotides encoding the last 15 amino acidresidues Cys-49 to Asn-63 of the synthetic single-chain form of INSULIN(GYG). With these two primers, the synthetic single-chain INSULIN (GYG)protein was generated by annealing, extension of the annealed primers,digestion with Sal I and Cla I, and subcloning into Xho I/Cla I digestedpScCHSA. The Not I fragment from this clone was then ligated into theNot I site of pSAC35 to generate construct ID 2255. Construct ID #2255encodes an albumin fusion protein containing the chimeric leadersequence, the synthetic single-chain form of INSULIN (GYG), and themature form of HSA.

Further analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing should confirm the presence of theexpected INSULIN (GYG) sequence (see below).

INSULIN albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the synthetic single-chain analog of INSULIN, i.e., Phe-1to Asn-62; the sequence corresponding to the C-peptide in the middleregion of the proinsulin cDNA was replaced by the C-domain of InsulinGrowth Factor 1, “IGF-1” (GY³²GSSSRRAPQT, SEQ ID NO:2147). In oneembodiment of the invention, INSULIN albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature INSULINalbumin fusion protein is secreted directly into the culture medium.INSULIN albumin fusion proteins of the invention may compriseheterologous signal sequences including, but not limited to, MAF, INV,Ig, Fibulin B, Clusterin, Insulin-Like Growth Factor Binding Protein 4,variant HSA leader sequences including, but not limited to, a chimericHSA/MAF leader sequence, or other heterologous signal sequences known inthe art. In a preferred embodiment, INSULIN albumin fusion proteins ofthe invention comprise the native INSULIN. In further preferredembodiments, the INSULIN albumin fusion proteins of the inventionfurther comprise an N-terminal methionine residue. Polynucleotidesencoding these polypeptides, including fragments and/or variants, arealso encompassed by the invention.

Expression and Purification of Construct ID 2255.

Expression in Yeast S. cerevisiae.

Construct 2255 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted INSULIN (GYG) albuminfusion protein expressed from construct ID #2255 in yeast S. cerevisiaecan be purified as described in Example 4. N-terminal sequencing of theexpressed and purified albumin fusion protein should generate FVNQHwhich corresponds to the amino terminus of the synthetic single-chainlong-acting insulin analog (INSULIN (GY³²G)).

In Vitro 1³H1-2-Deoxyglucose Uptake Assay in the Presence of the AlbuminFusion Protein Encoded by Construct 2255. Method

The in vitro assay to measure the glucose uptake in 3T3-L1 adipocytes inthe presence of the INSULIN (GYG) albumin fusion protein encoded byconstruct 2255 can be carried out as described below in Example 41.Other assays known in the art that may be used to test INSULIN (GYG)albumin fusion proteins' include, but are not limited to, L6 RatMyoblast Proliferation Assay via glycogen synthase kinase-3 (GSK-3) andH4IIe reporter assays (see Example 48) including the rat Malic EnzymePromoter (rMEP)-SEAP, Sterol Regulatory Element Binding Protein(SREBP)-SEAP, Fatty Acid Synthetase (FAS)-SEAP, and PhosphoEnolPyruvateCarboxyKinase (PEPCK)-SEAP reporters.

In Vitro Pancreatic Cell-Lines Proliferation Assay in the Presence ofthe Albumin Fusion Protein Encoded by Construct 2255. Method

The in vitro assay to measure the differentiation and proliferation ofductal epithelium pancreatic ARIP cell-line into insulin-producing betacells and/or to measure the proliferation of the insulin-producing RIN-Mbeta cell-line in the presence of the INSULIN (GYG) albumin fusionprotein encoded by construct 2255 can be carried out as described belowunder heading: “Example 42: In vitro Assay of [³H]-ThymidineIncorporation into Pancreatic Cell-lines”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2255 canbe Assayed In Vivo Using Diabetic NOD and/or NIDDM Mouse Models.

The activity of the INSULIN (GYG) albumin fusion protein encoded byconstruct 2255 can be measured using NOD and/or NIDDM mouse modelsdescribed below under the headings, “Example 44: Occurrence of Diabetesin NOD Mice”, “Example 45: Histological Examination of NOD Mice”, and“Example 47: In vivo Mouse Model of NIDDM”.

Example 35 Construct ID 2276, HSA-Insulin (GGG), Generation

Construct ID 2276, pSAC35.HSA.INSULIN(GGG).F1-N58, encodes for anHSA-INSULIN (GGG) fusion protein which comprises full length HSA,including the native HSA leader sequence fused to the amino-terminus ofthe synthetic single-chain long-acting insulin analog (INSULIN (GG³²G))with a Gly at position 32, cloned into the yeast S. cerevisiaeexpression vector pSAC35.

Cloning of INSULIN (GGG) cDNA for Construct 2276.

The DNA encoding the synthetic single-chain form of INSULIN (GGG) wasPCR generated using four overlapping primers. The sequence correspondingto the C-peptide in the middle region of the proinsulin cDNA wasreplaced by the synthetic linker “GG³²GPGKR” (SEQ ID NO:2148) to avoidthe need for proinsulin processing and to ensure proper folding of thesingle-chain protein. The sequence was codon optimized for expression inyeast S. cerevisiae. The PCR fragment was digested and subcloned intoBsu 361/Asc I digested pScNHSA. A Not I fragment was then subcloned intothe pSAC35 plasmid. Construct ID #2276 encodes for full length HSA,including the native HSA leader sequence fused to the amino-terminus ofthe synthetic single-chain form of INSULIN (GGG).

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the syntheticsingle-chain form of INSULIN (GGG), INSULIN (GGG)-1 and INSULIN (GGG)-2,were synthesized:

INSULIN (GGG)-5: (SEQ ID NO: 901)5′-GTCAAGCTGCCTTAGGCTTATTCGTTAACCAACACTTGTGTGGTTCTCACTTGGTTGAAGCTTTGTACTTGGTTTGTGGTGAA-3′ INSULIN (GGG)-6: (SEQ ID NO:902) 5′-ATCGCATATGGCGCGCCCTATTAGTTACAGTAGTTTTCCAATTGGTACAAAGAACAAATAGAAGTACAA-3′

INSULIN (GGG)-5 incorporates a Bsu 36I cloning site (shown in italics)and encodes the first 21 amino acids (shown in bold) of the ORF of thesynthetic single-chain form of INSULIN (GGG). In INSULIN (GGG)-6, theitalicized sequence is an Asc I site. In INSULIN (GGG)-6, the boldedsequence is the reverse complement of the last 49 nucleotides encodingamino acid residues Cys-44 to Asn-58 of the synthetic single-chain formof INSULIN (GGG). With these two primers, the synthetic single-chainform of INSULIN (GGG) was PCR amplified. Annealing and extensiontemperatures and times must be empirically determined for each specificprimer pair and template.

The PCR product was purified (for example, using Wizard PCR Preps DNAPurification System (Promega Corp)) and then digested with Bsu36I andAscI. After further purification of the Bsu36I-AscI fragment by gelelectrophoresis, the product was cloned into Bsu36I/AscI digestedpScNHSA. A Not I fragment was further subcloned into pSAC35 to giveconstruct ID #2276.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing should confirm the presence of theexpected mature HSA sequence (see below).

INSULIN albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the synthetic single-chain analog of INSULIN, i.e., Phe-1to Asn-58; the sequence corresponding to the C-peptide in the middleregion of the proinsulin cDNA was replaced by the synthetic linker“GG³²GPGKR” (SEQ ID NO:2148). In one embodiment of the invention,INSULIN albumin fusion proteins of the invention further comprise asignal sequence which directs the nascent fusion polypeptide in thesecretory pathways of the host used for expression. In a furtherpreferred embodiment, the signal peptide encoded by the signal sequenceis removed, and the mature INSULIN albumin fusion protein is secreteddirectly into the culture medium. INSULIN albumin fusion proteins of theinvention may comprise heterologous signal sequences including, but notlimited to, MAF, INV, Ig, Fibulin B, Clusterin, Insulin-Like GrowthFactor Binding Protein 4, variant HSA leader sequences including, butnot limited to, a chimeric HSA/MAF leader sequence, or otherheterologous signal sequences known in the art. In a preferredembodiment, INSULIN albumin fusion proteins of the invention comprisethe native INSULIN. In further preferred embodiments, the INSULINalbumin fusion proteins of the invention further comprise an N-terminalmethionine residue. Polynucleotides encoding these polypeptides,including fragments and/or variants, are also encompassed by theinvention.

Expression and Purification of Construct ID 2276.

Expression in Yeast S. cerevisiae.

Construct 2276 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted INSULIN (GGG) albuminfusion protein expressed from construct ID #2276 in yeast S. cerevisiaecan be purified as described in Example 4. N-terminal sequencing shouldyield DARKS (SEQ ID NO:2143) which corresponds to the amino terminus ofthe mature form of HSA.

In Vitro [³H]-2-Deoxyglucose Uptake Assay in the Presence of the AlbuminFusion Protein Encoded by Construct 2276. Method

The in vitro assay to measure the glucose uptake in 3T3-L1 adipocytes inthe presence of the INSULIN (GGG) albumin fusion protein encoded byconstruct 2276 was carried out as described below in Example 41. Otherassays known in the art that may be used to test INSULIN (GGG) albuminfusion proteins' include, but are not limited to, L6 Rat MyoblastProliferation Assay via glycogen synthase kinase-3 (GSK-3) and H4IIereporter assays (see Example 48) including the rat Malic Enzyme Promoter(rMEP)-SEAP, Sterol Regulatory Element Binding Protein (SREBP)-SEAP,Fatty Acid Synthetase (FAS)-SEAP, and PhosphoEnolPyruvate CarboxyKinase(PEPCK)-SEAP reporters.

Result

The supernatant derived from transformed yeast S. cerevisiae expressinginsulin albumin fusion encoded by construct 2276 demonstrated glucoseuptake/transport activity in 3T3-L1 adipocytes (see FIG. 18).

In Vitro Pancreatic Cell-Lines Proliferation Assay in the Presence ofthe Albumin Fusion Protein Encoded by Construct 2276. Method

The in vitro assay to measure the differentiation and proliferation ofductal epithelium pancreatic ARIP cell-line into insulin-producing betacells and/or to measure the proliferation of the insulin-producing RIN-Mbeta cell-line in the presence of the INSULIN (GGG) albumin fusionprotein encoded by construct 2276 can be carried out as described belowunder heading: “Example 42: In vitro Assay of [³H]-ThymidineIncorporation into Pancreatic Cell-lines”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2276 canbe Assayed In Vivo Using Diabetic NOD and/or NIDDM Mouse Models.

The activity of the INSULIN (GGG) albumin fusion protein encoded byconstruct 2276 can be measured using NOD and/or NIDDM mouse modelsdescribed below under the headings, “Example 44: Occurrence of Diabetesin NOD Mice”, “Example 45: Histological Examination of NOD Mice”, and“Example 47: In vivo Mouse Model of NIDDM”.

Example 36 Construct ID 2278, Insulin (GGG)-HSA, Generation

Construct ID 2278, pSAC35.INSULIN(GGG).HSA, encodes for an INSULIN(GGG)-HSA fusion protein which comprises the HSA chimeric leadersequence of HSA fused to the amino-terminus of the syntheticsingle-chain long-acting insulin analog (INSULIN (GG³²G)) with a Gly inposition 32, which is, in turn, fused to the mature form of HSA, clonedinto the yeast S. cerevisiae expression vector pSAC35.

Cloning of INSULIN (GGG) cDNA for Construct 2278.

The DNA encoding the synthetic single-chain form of INSULIN (GGG) wasPCR generated using four overlapping primers. The sequence correspondingto the C-peptide in the middle region of the proinsulin cDNA wasreplaced by the synthetic linker “GG³²GPGKR” (SEQ ID NO:2148) to avoidthe need for proinsulin processing and to ensure proper folding of thesingle-chain protein. The sequence was codon optimized for expression inyeast S. cerevisiae. The PCR fragment was digested with Sal I/Cla I andsubcloned into Xho I/Cla I digested pScCHSA. A Not I fragment was thensubcloned into the pSAC35 plasmid. Construct ID #2278 encodes for thechimeric leader sequence of HSA fused to the amino-terminus of thesynthetic single-chain form of INSULIN (GGG) followed by the mature formof HSA.

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the syntheticsingle-chain form of INSULIN (GGG), INSULIN (GGG)-7 and INSULIN (GGG)-8,were synthesized:

INSULIN (GGG)-7: (SEQ ID NO: 903)5′-TCCAGGAGCGTCGACAAAAGATTCGTTAACCAACACTTGTGTGGTTCTCACTTGGTTGAAGCTTTGTACTTGGTTTGTGGTGAA-3′ INSULIN (GGG)-8: (SEQ ID NO:904) 5′-AGACTTTAAATCGATGAGCAACCTCACTCTTGTGTGCATCGTTACAGTAGTTTTCCAATTGGTACAAAGAACAAATAGAAGTACAA-3′

INSULIN (GGG)-7 incorporates a Sal I cloning site (shown in italics) andthe DNA encoding the first 21 amino acids (shown in bold) of the ORF ofthe synthetic single-chain form of INSULIN(GGG). In INSULIN (GGG)-8, theitalicized sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein. The bolded sequence is thereverse complement of the 46 nucleotides encoding the last 15 amino acidresidues Cys-44 to Asn-58 of the synthetic single-chain form of INSULIN(GGG). With these two primers, the synthetic single-chain INSULIN (GGG)protein was generated by annealing, extension of the annealed primers,digestion with Sal I and Cla I, and subcloning into Xho I/Cla I digestedpScCHSA. The Not I fragment from this clone was then ligated into theNot I site of pSAC35 to generate construct ID 2278. Construct ID #2278encodes an albumin fusion protein containing the chimeric leadersequence, the synthetic single-chain form of INSULIN (GGG), and themature form of HSA.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing should confirm the presence of theexpected INSULIN (GGG) sequence (see below).

INSULIN albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the synthetic single-chain analog of INSULIN, i.e., Phe-1to Asn-58; the sequence corresponding to the C-peptide in the middleregion of the proinsulin cDNA was replaced by the synthetic linker“GG³²GPGKR” (SEQ ID NO:2148). In one embodiment of the invention,INSULIN albumin fusion proteins of the invention further comprise asignal sequence which directs the nascent fusion polypeptide in thesecretory pathways of the host used for expression. In a furtherpreferred embodiment, the signal peptide encoded by the signal sequenceis removed, and the mature INSULIN albumin fusion protein is secreteddirectly into the culture medium. INSULIN albumin fusion proteins of theinvention may comprise heterologous signal sequences including, but notlimited to, MAF, INV, Ig, Fibulin B, Clusterin, Insulin-Like GrowthFactor Binding Protein 4, variant HSA leader sequences including, butnot limited to, a chimeric HSA/MAF leader sequence, or otherheterologous signal sequences known in the art. In a preferredembodiment, INSULIN albumin fusion proteins of the invention comprisethe native INSULIN. In further preferred embodiments, the INSULINalbumin fusion proteins of the invention further comprise an N-terminalmethionine residue. Polynucleotides encoding these polypeptides,including fragments and/or variants, are also encompassed by theinvention.

Expression and Purification of Construct ID 2278.

Expression in Yeast S. cerevisiae.

Construct 2278 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted INSULIN (GGG) albuminfusion protein expressed from construct ID #2278 in yeast S. cerevisiaecan be purified as described in Example 4. N-terminal sequencing of theexpressed and purified albumin fusion protein should generate FVNQH (SEQID NO:2149) which corresponds to the amino terminus of the syntheticsingle-chain long-acting insulin analog (INSULIN (GG³²G)).

In Vitro [³H]-2-Deoxyglucose Uptake Assay in the Presence of the AlbuminFusion Protein Encoded by Construct 2278. Method

The in vitro assay to measure the glucose uptake in 3T3-L1 adipocytes inthe presence of the INSULIN (GGG) albumin fusion protein encoded byconstruct 2278 can be carried out as described below in Example 41.Other assays known in the art that may be used to test INSULIN (GGG)albumin fusion proteins' include, but are not limited to, L6 RatMyoblast Proliferation Assay via glycogen synthase kinase-3 (GSK-3) andH4IIe reporter assays (see Example 48) including the rat Malic EnzymePromoter (rMEP)-SEAP, Sterol Regulatory Element Binding Protein(SREBP)-SEAP, Fatty Acid Synthetase (FAS)-SEAP, and PhosphoEnolPyruvateCarboxyKinase (PEPCK)-SEAP reporters.

In Vitro Pancreatic Cell-Lines Proliferation Assay in the Presence ofthe Albumin Fusion Protein Encoded by Construct 2278. Method

The in vitro assay to measure the differentiation and proliferation ofductal epithelium pancreatic ARIP cell-line into insulin-producing betacells and/or to measure the proliferation of the insulin-producing RIN-Mbeta cell-line in the presence of the INSULIN (GGG) albumin fusionprotein encoded by construct 2278 can be carried out as described belowunder heading: “Example 42: In vitro Assay of [³H]-ThymidineIncorporation into Pancreatic Cell-lines”.

The Activity of the Albumin Fusion Protein Encoded by Construct 2278 canbe Assayed In Vivo Using Diabetic NOD and/or NIDDM Mouse Models.

The activity of the INSULIN (GGG) albumin fusion protein encoded byconstruct 2278 can be measured using NOD and/or NIDDM mouse modelsdescribed below under the headings, “Example 44: Occurrence of Diabetesin NOD Mice”, “Example 45: Histological Examination of NOD Mice”, and“Example 47: In vivo Mouse Model of NIDDM”.

Example 37 Indications for Insulin Albumin Fusion Proteins

Results from in vitro assays described above indicate that insulinalbumin fusion proteins are useful for the treatment, prevention, and/ordiagnosis of hyperglycemia, insulin resistance, insulin deficiency,hyperlipidemia, hyperketonemia, and diabetes mellitus, Type 1 and Type 2diabetes.

Example 38 Preparation of HSA-hGH Fusion Proteins

An HSA-hGH fusion protein was prepared as follows:

Cloning of hGH cDNA

The hGH cDNA was obtained from a human pituitary gland cDNA library(catalogue number HL1097v, Clontech Laboratories, Inc) by PCRamplification. Two oligonucleotides suitable for PCR amplification ofthe hGH cDNA, HGH1 and HGH2, were synthesized using an AppliedBiosystems 380B Oligonucleotide Synthesizer.

(SEQ ID NO: 1020) HGH1: 5′-CCCAAGAATTCCCTTATCCAGGC-3′ (SEQ ID NO: 1021)HGH2: 5′-GGGAAGCTTAGAAGCCACAGGATCCCTCCACAG-3′

HGH 1 and HGH2 differed from the equivalent portion of the hGH cDNAsequence (Martial et. al., 1979) by two and three nucleotides,respectively, such that after PCR amplification an EcoRI site would beintroduced to the 5′ end of the cDNA and a BamHI site would beintroduced into the 3′ end of the cDNA. In addition, HGH2 contained aHindIII site immediately downstream of the hGH sequence.

PCR amplification using a Perkin-Elmer-Cetus Thermal Cycler 9600 and aPerkin-Elmer-Cetus PCR kit, was performed using single-stranded DNAtemplate isolated from the phage particles of the cDNA library asfollows: 10 μL phage particles were lysed by the addition of 10 μL phagelysis buffer (280 μg/mL proteinase K in TE buffer) and incubation at 55°C. for 15 min followed by 85° C. for 15 min. After a 1 min. incubationon ice, phage debris was pelleted by centrifugation at 14,000 rpm for 3min. The PCR mixture contained 6 μL of this DNA template, 0.1 μM of eachprimer and 200 μM of each deoxyribonucleotide. PCR was carried out for30 cycles, denaturing at 94° C. for 30 s, annealing at 65° C. for 30 sand extending at 72° C. for 30 s, increasing the extension time by 1 sper cycle.

Analysis of the reaction by gel electrophoresis showed a single productof the expected size (589 base pairs).

The PCR product was purified using Wizard PCR Preps DNA PurificationSystem (Promega Corp) and then digested with EcoR1 and HindIII. Afterfurther purification of the EcoR1-HindIII fragment by gelelectrophoresis, the product was cloned into pUC19 (GIBCO BRL) digestedwith EcoRI and HindIII, to give pHGH1. DNA sequencing of the EcoR1HindIII region showed that the PCR product was identical in sequence tothe hGH sequence (Martial et al., 1979), except at the 5′ and 3′ ends,where the EcoR1 and BamHI sites had been introduced, respectively.

Expression of the hGH cDNA.

The polylinker sequence of the phagemid pBluescribe (+) (Stratagene) wasreplaced by inserting an oligonucleotide linker, formed by annealing two75-mer oligonucleotides, between the EcoRI and HindIII sites to formpBST(+). The new polylinker included a unique NotI site.

The NotI HSA expression cassette of pAYE309 (EP 431 880) comprising thePRBI promoter, DNA encoding the HSA/MFα-1 hybrid leader sequence, DNAencoding HSA and the ADH1 terminator, was transferred to pBST(+) to formpHSA1. The HSA coding sequence was removed from this plasmid bydigestion with Hind III followed by religation to form pHSA2.

Cloning of the hGH cDNA provided the hGH coding region lacking thepro-hGH sequence and the first 8 base pairs (bp) of the mature hGHsequence. In order to construct an expression plasmid for secretion ofhGH from yeast, a yeast promoter, signal peptide and the first 8 bp ofthe hGH sequence were attached to the 5′ end of the cloned hGH sequenceas follows: The HindIII-SfaNI fragment from pHSA 1 was attached to the5′ end of the EcoRI/HindIII fragment from pHGHI via two syntheticoligonucleotides, HGH3 and HGH4 (which can anneal to one another in sucha way as to generate a double stranded fragment of DNA with sticky endsthat can anneal with SfaNI and EcoRI sticky ends):

(SEQ ID NO: 1023) HGH3: 5′-GATAAAGATTCCCAAC-3′ (SEQ ID NO: 1024) HGH4:5′-AATTGTTGGGAATCTTT-3′

The Hind III fragment so formed was cloned into HindIII-digested pHSA2to make pHGH2, such that the hGH cDNA was positioned downstream of thePRBI promoter and HSA/1/MFα-1 fusion leader sequence (see, InternationalPublication No. WO 90/01063). The NotI expression cassette contained inpHGH2, which included the ADH1 terminator downstream of the hGH cDNA,was cloned into NotI-digested pSAC35 (Sleep et al., BioTechnology 8:42(1990)) to make pHGH12. This plasmid comprised the entire 2 μm plasmidto provide replication functions and the LEU2 gene for selection oftransformants.

pHGH12 was introduced into S. cerevisiae D88 by transformation andindividual transformants were grown for 3 days at 30° C. in 10 mL YEPD(1% w/v yeast extract, 2% w/v, peptone, 2% w/v, dextrose).

After centrifugation of the cells, the supernatants were examined bySDS-polyacrylamide gel electrophoresis (SDS-PAGE) and were found tocontain protein which was of the expected size and which was recognizedby anti-hGH antiserum (Sigma, Poole, UK) on Western blots.

Cloning and Expression of an HSA-hGH Fusion Protein.

In order to fuse the HSA cDNA to the 5′ end of the hGH cDNA, the pHSA1HindIII-Bsu361 fragment (containing most of the HSA cDNA) was joined tothe pHGH1 EcoRI-HindIII fragment (containing most of the hGH cDNA) viatwo oligonucleotides, HGH7 and HGH8

(SEQ ID NO: 1025) HGH7: 5′-TTAGGCTTATTCCCAAC 3′ (SEQ ID NO: 1026) HGH8:5′-AATTGTTGGGAATAAGCC 3′

The HindIII fragment so formed was cloned into pHSA2 digested withHindIII to make pHGH10, and the NotI expression cassette of this plasmidwas cloned into NotI-digested pSAC35 to make pHGH16.

pHGH16 was used to transform S. cerevisiae D88 and supernatants ofcultures were analyzed as described above. A predominant band wasobserved that had a molecular weight of approximately 88 kD,corresponding to the combined masses of HSA and hGH. Western blottingusing anti-HSA and anti-hGH antisera (Sigma) confirmed the presence ofthe two constituent parts of the albumin fusion protein.

The albumin fusion protein was purified from culture supernatant bycation exchange chromatography, followed by anion exchange and gelpermeation chromatography. Analysis of the N-terminus of the protein byamino acid sequencing confirmed the presence of the expected albuminsequence.

An in vitro growth hormone activity assay (Ealey et al., GrowthRegulation 5:36 (1995)) indicated that the albumin fusion proteinpossessed full hGH activity. In a hypophysectomised rat weight gainmodel, performed essentially as described in the European Pharmacopoeia(1987, monograph 556), the fusion molecule was more potent than hGH whenthe same number of units of activity (based on the above in vitro assay)were administered daily. Further experiments in which the albumin fusionprotein was administered once every four days showed a similar overallgrowth response to a daily administration of hGH. Pharmacokineticexperiments in which ¹²⁵I-labeled protein was administered to ratsindicated an approximately ten-fold increase in circulatory half-lifefor the albumin fusion protein compared to hGH.

A similar plasmid was constructed in which DNA encoding the S.cerevisiae invertase (SUC2) leader sequence replaced the sequence forthe hybrid leader, such that the encoded leader and the junction) withthe HSA sequence were as follows:

(SEQ ID NO: 1027) ... MLLQAFLFLLAGFAAKISA ↓ DAHKS ..... Invertaseleader         HSA sequence ...

On introduction into S. cerevisiae DBI, this plasmid directed theexpression and secretion of the albumin fusion protein at a levelsimilar to that obtained with pHGH16. Analysis of the N-terminus of thealbumin fusion protein indicated precise and efficient cleavage of theleader sequence from the mature protein.

Cloning and Expression of an hGH-HSA Fusion Protein.

In order to fuse the hGH cDNA to the 5′ end of the HSA cDNA, the HSAcDNA was first altered by site-directed mutagenesis to introduce anEcoN1 site near the 5′ end of the coding region. This was done by themethod of Kunkel et al. (Methods in Enzymol. 154:367 (1987)) usingsingle-stranded DNA template prepared from pHSAI and a syntheticoligonucleotide, LEU4:

(SEQ ID NO: 1028) LEU4: 5′-GAGATGCACACCTGAGTGAGG-3′Site-directed mutagenesis using this oligonucleotide changed the codingsequence of the HSA cDNA from Lys4 to Leu4 (K4L). However, this changewas repaired when the hGH cDNA was subsequently joined at the 5′ end bylinking the pHGH2 Not1-BamHI fragment to the EcoNI-NotI fragment of themutated pHSAI, via the two oligonucleotides HGH5 and HGH6:

(SEQ ID NO: 1029) HGH5: 5′-GATCCTGTGGCTTCGATGCACACAAGA-3′ (SEQ ID NO:1030) HGH6: 5′-CTCTTGTGTGCATCGAAGCCACAG-3′

The Not1 fragment so formed was cloned into Not1-digested pSAC35 to makepHGH14. pHGH14 was used to transform S. cerevisiae D88 and supernatantsof culture were analyzed as above. A predominant band was observed thathad a molecular weight of approximately 88 kD, corresponding to thecombined masses of hGH and HSA. Western blotting using anti-HSA andanti-hGH antisera confirmed the presence of the two constituent parts ofthe albumin fusion protein.

The albumin fusion protein was purified from culture supernatant bycation exchange chromatography, followed by anion exchange and gelpermeation chromatography. Analysis of the N-terminus of the protein byamino acid sequencing confirmed the presence of the expected hGHsequence.

In vitro studies showed that the albumin fusion protein retained hGHactivity, but was significantly less potent than an albumin fusionprotein comprising full length HSA (1-585) as the N-terminal portion andhGH as the C-terminal portion, as described above.

Construction of Plasmids for the Expression of hGH Fusions to Domains ofHSA.

Fusion polypeptides were made in which the hGH molecule was fused to thefirst two domains of HSA (residues 1 to 387). Fusion to the N terminusof hGH was achieved by joining the pHSA1 HindIII-SapI fragment, whichcontained most of the coding sequence for domains 1 and 2 of HSA, to thepHGHI EcoRI-HindIII fragment, via the oligonucleotides HGH 11 and HGH12:

HGH11: (SEQ ID NO: 1031) 5′-TGTGGAAGAGCCTCAGAATTTATTCCCAAC-3′ HGH12:(SEQ ID NO: 1032) 5′-AATTGTTGGGAATAAATTCTGAGGCTCTTCC-3′

The HindIII fragment so formed was cloned into HindIII-digested pHSA2 tomake pHGH37 and the NotI expression cassette of this plasmid was clonedinto NotI-digested pSAC35.

The resulting plasmid, pHGH38, contained an expression cassette that wasfound to direct secretion of the fusion polypeptide into the supernatantwhen transformed into S. cerevisiae DB 1. Western blotting usinganti-HSA and anti-hGH antisera confirmed the presence of the twoconstituent parts of the albumin fusion protein.

The albumin fusion protein was purified from culture supernatant bycation exchange chromatography followed by gel permeationchromatography.

In vivo studies with purified protein indicated that the circulatoryhalf-life was longer than that of hGH, and similar to that of an albuminfusion protein comprising full-length HSA (1-585) as the N-terminalportion and hGH as the C-terminal portion, as described above. In vitrostudies showed that the albumin fusion protein retained hGH activity.

Using a similar strategy as detailed above, an albumin fusion proteincomprising the first domain of HSA (residues 1-194) as the N-terminalportion and hGH as the C-terminal portion, was cloned and expressed inS. cerevisiae DBL. Western blotting of culture supernatant usinganti-HSA and anti-hGH antisera confirmed the presence of the twoconstituent parts of the albumin fusion protein.

Fusion of HSA to hGH Using a Flexible Linker Sequence

Flexible linkers, comprising repeating units of[Gly-Gly-Gly-Gly-Ser]_(n), (SEQ ID NO:2150) where n was either 2 or 3,were introduced between the HSA and hGH albumin fusion protein bycloning of the oligonucleotides HGH16, HGH17, HGH18 and HGH19:

HGH16: (SEQ ID NO: 1133) 5′-TTAGGCTTAGGTGGCGGTGGATCCGGCGGTGGTGGATCTTTCCCAAC-3′ HGH17: (SEQ ID NO: 1134)5′-AATTGTTGGGAAAGATCCACCACCGCCGGATCCACCGCCACCTA AGCC-3′ HGH18: (SEQ IDNO: 1135) 5′-TTAGGCTTAGGCGGTGGTGGATCTGGTGGCGGCGGATCTGGTGGCGGTGGATCCTTCCCAAC-3′ HGH19: (SEQ ID NO: 1136)5′-AATTGTTGGGAAGGATCCACCGCCACCAGATCCGCCGCCACCAG ATCCACCACCGCCTAAGCC-3′

Annealing of HGH16 with HGH17 resulted in n=2, while HGH18 annealed toHGH19 resulted in n=3. After annealing, the double-strandedoligonucleotides were cloned with the EcoRI-Bsu361 fragment isolatedfrom pHGH1 into Bsu361-digested pHGH10 to make pHGH56 (where n=2) andpHGH57 (where n=3). The NotI expression cassettes from these plasmidswere cloned into NotI-digested pSAC35 to make pHGH58 and pHGH59,respectively.

Cloning of the oligonucleotides to make pHGH56 and pHGH57 introduced aBamHI site in the linker sequences. It was therefore possible toconstruct linker sequences in which n=1 and n=4, by joining either theHindIII-BamHI fragment from pHGH56 to the BamHI-HindIII fragment frompHGH57 (making n=1), or the HindIII-BamHI fragment from pHGH57 to theBamHI-HindIII fragment from pHGH56 (making n=2). Cloning of thesefragments into the Hind III site of pHSA2, resulted in pHGH60 (n=1) andpHGH61 (n=4). The NotI expression cassettes from pHGH60 and pHGH61 werecloned into NotI-digested pSAC35 to make pHGH62 and pHGH63,respectively.

Transformation of S. cerevisiae with pHGH58, pHGH59, pHGH62 and pHGH63resulted in transformants that secreted the fusion polypeptides into thesupernatant. Western blotting using anti-HSA and anti-hGH antiseraconfirmed the presence of the two constituent parts of the albuminfusion proteins.

The albumin fusion proteins were purified from culture supernatant bycation exchange chromatography, followed by anion exchange and gelpermeation chromatography. Analysis of the N-termini of the proteins byamino acid sequencing confirmed the presence of the expected albuminsequence. Analysis of the purified proteins by electrospray massspectrometry confirmed an increase in mass of 315 D (n=1), 630 D (n=2),945 D (n=3) and 1260 D (n=4) compared to the HSA-hGH fusion proteindescribed above. The purified protein was found to be active in vitro.

hGH albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the mature form of hGH. In one embodiment of theinvention, hGH albumin fusion proteins of the invention further comprisea signal sequence which directs the nascent fusion polypeptide in thesecretory pathways of the host used for expression. In a furtherpreferred embodiment, the signal peptide encoded by the signal sequenceis removed, and the mature hGH albumin fusion protein is secreteddirectly into the culture medium. hGH albumin fusion proteins of theinvention may comprise heterologous signal sequences including, but notlimited to, MAF, INV, Ig, Fibulin B, Clusterin, Insulin-Like GrowthFactor Binding Protein 4, variant HSA leader sequences including, butnot limited to, a chimeric HSA/MAF leader sequence, or otherheterologous signal sequences known in the art. In a preferredembodiment, hGH albumin fusion proteins of the invention comprise thenative hGH. In further preferred embodiments, the hGH albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Increased Shelf-Life of HSA-hGH Fusion Proteins: Methods

HSA-hGH and hGH were separately diluted in cell culture media containing5% horse serum to final concentrations of 100-200 μg/ml and incubated at4, 37 or 50° C. At time zero and at weekly intervals thereafter,aliquots of the samples were tested for their biological activity in theNb2 cell proliferation assay, and the data normalized to the biologicalactivity of the control (hGH solution at time zero). In other assays hGHand HSA-hGH were incubated in phosphate buffer saline in at 4, 37 and 50degree C.

Nb2 cell proliferation assay: The growth of these cells is dependent onhGH or other lactogenic hormones. In a typical experiment 10⁴ cells/wellare plated in 96-well plate in the presence of different concentrationof hGH or HSA-hGH in media such as DMEM containing 5-10% horse serum for24-48 hrs in the incubator. After the incubation period, 1:10 volume ofMTT (5 mg/ml in H₂O) is added to each well and the plate is incubatedfor a further 6-16 hrs. The growing cells convert MTT to insolubleformazan. The formazan is solublized by acidic isopropanol, and thecolor produced is measured at 570 nm on microtiter plate reader. Theextent of formazan formation reflects the level of cellularproliferation.

Increased Shelf-Life of HSA-hGH Fusion Proteins: Results

The fusion of Therapeutic proteins to albumin confers stability inaqueous or other solution. The shelf-life of an HSA fusion protein isextended in terms of the biological activity of HSA-hGH remaining afterstorage in cell culture media for up to 5 weeks at 37° C. A solution of200 μg/ml HSA-hGH was prepared in tissue culture media containing 5%horse serum, and the solution incubated at 37° C. starting at time zero.At the indicated times, a sample was removed and tested for itsbiological activity in the Nb2 cell assay, at 2 ng/ml finalconcentration. The biological activity of HSA-hGH remains essentiallyintact (within experimental variation) after 5 weeks of incubation at37° C. The recombinant hGH used as control for this experiment lost itsbiological activity in the first week of the experiment.

After storage in cell culture media for up to 3 weeks at 4, 37, or 50°C., HSA-hGH was stable. At time zero, a solution of HSA-hGH was preparedin tissue culture media containing 5% horse serum, and incubated at 4,37, and 50° C. At the indicated periods a sample was removed and assayedfor its biological activity in the Nb2 cell proliferation assay, at 60ng/ml final concentration. HSA-hGH retains over 90% of its initialactivity at all temperatures tested for at least 3 weeks afterincubation while hGH loses its biological activity within the firstweek. This level of activity is further retained for at least 7 weeks at37° C. and 5 weeks at 50° C. These results indicate that HSA-hGH ishighly stable in aqueous solution even under temperature stress.

The biological activity of HSA-hGH was stable compared to hGH in the Nb2cell proliferation assay. Nb2 cells were grown in the presence ofincreasing concentrations of recombinant hGH or HSA-hGH, added at timezero. The cells were incubated for 24 or 48 hours before measuring theextent of proliferation by the MTT method. The increased stability ofHSA-hGH in the assay results in essentially the same proliferativeactivity at 24 hours as at 48 hours while hGH shows a significantreduction in its proliferative activity after 48 hours of incubation.Compared to hGH, the HSA-hGH has lower biological potency after 1 day;the albumin fusion protein is about 5 fold less potent than hGH.However, after 2 days the HSA-hGH shows essentially the same potency ashGH due to the short life of hGH in the assay. This increase in thestability of the hGH as an albumin fusion protein has a major unexpectedimpact on the biological activity of the protein.

Example 39 Indications for hGH Albumin Fusion Proteins

Results from in vitro and in vivo assays indicate that hGH albuminfusion proteins can be used to treat, prevent, detect, diagnose, and/orameliorate acromegaly, growth failure, growth failure and endogenousgrowth hormone replacement, growth hormone deficiency, growth failure orgrowth retardation Prader-Willi syndrome in children 2 years or older,growth deficiencies, growth failure associated with chronic renalinsufficiency, postmenopausal osteoporosis, burns, cachexia, cancercachexia, dwarfism, metabolic disorders, obesity, renal failure,Turner's Syndrome (pediatric and adult), fibromyalgia, fracturetreatment, frailty, or AIDS wasting.

Example 40 Isolation of a Selected cDNA Clone from the Deposited Sample

Many of the albumin fusion constructs of the invention have beendeposited with the ATCC as shown in Table 3. The albumin fusionconstructs may comprise any one of the following expression vectors: theyeast S. cerevisiae expression vector pSAC35, the mammalian expressionvector pC4, or the mammalian expression vector pEE12.1.

pSAC35 (Sleep et al., 1990, Biotechnology 8:42), pC4 (ATCC Accession No.209646; Cullen et al., Molecular and Cellular Biology, 438-447 (1985);Boshart et al., Cell 41: 521-530 (1985)), and pEE12.1 (Lonza Biologics,Inc.; Stephens and Cockett, Nucl. Acids Res. 17: 7110 (1989);International Publication #WO89/01036; Murphy et al., Biochem J. 227:277-279 (1991); Bebbington et al., Bio/Technology 10:169-175 (1992);U.S. Pat. No. 5,122,464; International Publication #WO86/05807) vectorscomprise an ampicillin resistance gene for growth in bacterial cells.These vectors and/or an albumin fusion construct comprising them can betransformed into an E. coli strain such as Stratagene XL-1 Blue(Stratagene Cloning Systems, Inc., 11011 N. Torrey Pines Road, La Jolla,Calif., 92037) using techniques described in the art such as Hanahan,spread onto Luria-Broth agar plates containing 100 μg/mL ampicillin, andgrown overnight at 37° C.

The deposited material in the sample assigned the ATCC Deposit Numbercited in Table 3 for any given albumin fusion construct also may containone or more additional albumin fusion constructs, each encodingdifferent albumin fusion proteins. Thus, deposits sharing the same ATCCDeposit Number contain at least an albumin fusion construct identifiedin the corresponding row of Table 3.

Two approaches can be used to isolate a particular albumin fusionconstruct from the deposited sample of plasmid DNAs cited for thatalbumin fusion construct in Table 3.

Method 1: Screening

First, an albumin fusion construct may be directly isolated by screeningthe sample of deposited plasmid DNAs using a polynucleotide probecorresponding to SEQ ID NO:X for an individual construct ID number inTable 1, using methods known in the art. For example, a specificpolynucleotide with 30-40 nucleotides may be synthesized using anApplied Biosystems DNA synthesizer according to the sequence reported.The oligonucleotide can be labeled, for instance, with ³²P-γ-ATP usingT4 polynucleotide kinase and purified according to routine methods.(E.g., Maniatis et al., Molecular Cloning: A Laboratory Manual, ColdSpring Harbor Press, Cold Spring, N.Y. (1982)). The albumin fusionconstruct from a given ATCC deposit is transformed into a suitable host,as indicated above (such as XL-1 Blue (Stratagene)) using techniquesknown to those of skill in the art, such as those provided by the vectorsupplier or in related publications or patents cited above. Thetransformants are plated on 1.5% agar plates (containing the appropriateselection agent, e.g., ampicillin) to a density of about 150transformants (colonies) per plate. These plates are screened usingNylon membranes according to routine methods for bacterial colonyscreening (e.g., Sambrook et al., Molecular Cloning: A LaboratoryManual, 2nd Edit., (1989), Cold Spring Harbor Laboratory Press, pages1.93 to 1.104), or other techniques known to those of skill in the art.

Method 2: PCR

Alternatively, DNA encoding a given albumin fusion protein may beamplified from a sample of a deposited albumin fusion construct with SEQID NO:X, for example, by using two primers of 17-20 nucleotides thathybridize to the deposited albumin fusion construct 5′ and 3′ to the DNAencoding a given albumin fusion protein. The polymerase chain reactionis carried out under routine conditions, for instance, in 25 μl ofreaction mixture with 0.5 ug of the above cDNA template. A convenientreaction mixture is 1.5-5 mM MgCl₂, 0.01% (w/v) gelatin, 20 μM each ofdATP, dCTP, dGTP, dTTP, 25 pmol of each primer and 0.25 Unit of Taqpolymerase. Thirty five cycles of PCR (denaturation at 94° C. for 1 min;annealing at 55° C. for 1 min; elongation at 72° C. for 1 min) areperformed with a Perkin-Elmer Cetus automated thermal cycler. Theamplified product is analyzed by agarose gel electrophoresis and the DNAband with expected molecular weight is excised and purified. The PCRproduct is verified to be the selected sequence by subcloning andsequencing the DNA product.

Several methods are available for the identification of the 5′ or 3′non-coding portions of a gene which may not be present in the depositedclone. These methods include but are not limited to, filter probing,clone enrichment using specific probes, and protocols similar oridentical to 5′ and 3′ “RACE” protocols which are known in the art. Forinstance, a method similar to 5′ RACE is available for generating themissing 5′ end of a desired full-length transcript. (Fromont-Racine etal., Nucleic Acids Res., 21(7):1683-1684 (1993)).

Briefly, a specific RNA oligonucleotide is ligated to the 5′ ends of apopulation of RNA presumably containing full-length gene RNAtranscripts. A primer set containing a primer specific to the ligatedRNA oligonucleotide and a primer specific to a known sequence of thegene of interest is used to PCR amplify the 5′ portion of the desiredfull-length gene. This amplified product may then be sequenced and usedto generate the full length gene.

This above method starts with total RNA isolated from the desiredsource, although poly-A+ RNA can be used. The RNA preparation can thenbe treated with phosphatase if necessary to eliminate 5′ phosphategroups on degraded or damaged RNA which may interfere with the later RNAligase step. The phosphatase should then be inactivated and the RNAtreated with tobacco acid pyrophosphatase in order to remove the capstructure present at the 5′ ends of messenger RNAs. This reaction leavesa 5′ phosphate group at the 5′ end of the cap cleaved RNA which can thenbe ligated to an RNA oligonucleotide using T4 RNA ligase.

This modified RNA preparation is used as a template for first strandcDNA synthesis using a gene specific oligonucleotide. The first strandsynthesis reaction is used as a template for PCR amplification of thedesired 5′ end using a primer specific to the ligated RNAoligonucleotide and a primer specific to the known sequence of the geneof interest. The resultant product is then sequenced and analyzed toconfirm that the 5′ end sequence belongs to the desired gene.

Example 41 [³H]-2-Deoxyglucose Uptake Assay

Adipose, skeletal muscle, and liver are insulin-sensitive tissues.Insulin can stimulate glucose uptake/transport into these tissues. Inthe case of adipose and skeletal muscle, insulin initiates the signaltransduction that eventually leads to the translocation of the glucosetransporter 4 molecule, GLUT4, from a specialized intracellularcompartment to the cell surface. Once on the cell surface, GLUT4 allowsfor glucose uptake/transport.

[³H]-2-Deoxyglucose Uptake

A number of adipose and muscle related cell-lines can be used to testfor glucose uptake/transport activity in the absence or presence of acombination of any one or more of the therapeutic drugs listed for thetreatment of diabetes mellitus. In particular, the 3T3-L1 murinefibroblast cells and the L6 murine skeletal muscle cells can bedifferentiated into 3T3-L1 adipocytes and into myotubes, respectively,to serve as appropriate in vitro models for the [³H]-2-deoxyglucoseuptake assay (Urso et al., J Biol Chem, 274(43): 30864-73 (1999); Wanget al., J Mol Endocrinol, 19(3): 241-8 (1997); Haspel et al., J MembrBiol, 169 (1): 45-53 (1999); Tsakiridis et al., Endocrinology, 136(10):4315-22 (1995)). Briefly, 2×10⁵ cells/100 μL of adipocytes ordifferentiated L6 cells are transferred to 96-well Tissue-Culture, “TC”,treated, i.e., coated with 50 μg/mL of poly-L-lysine, plates inpost-differentiation medium and are incubated overnight at 37° C. in 5%CO₂. The cells are first washed once with serum free low glucose DMEMmedium and are then starved with 100 μL/well of the same medium and with100 μL/well of either buffer or of a combination of any one or more ofthe therapeutic drugs listed for the treatment of diabetes mellitus, forexample, increasing concentrations of 1 nM, 10 nM, and 100 nM of thetherapeutics of the subject invention (e.g., specific fusions disclosedas SEQ ID NO:Y and fragments and variants thereof) for 16 hours at 37°C. in the absence or presence of 1 nM insulin. The plates are washedthree times with 100 μL/well of HEPES buffered saline. Insulin is addedat 1 nM in HEPES buffered saline for 30 min at 37° C. in the presence of10 μM labeled [³H]-2-deoxyglucose (Amersham, #TRK672) and 10 μMunlabeled 2-deoxyglucose (SIGMA, D-3179). As control, the sameconditions are carried out except in the absence of insulin. A finalconcentration of 10 μM cytochalasin B (SIGMA, C6762) is added at 100μL/well in a separate well to measure the non-specific uptake. The cellsare washed three times with HEPES buffered saline. Labeled, i.e., 10 μMof [³H]-2-deoxyglucose, and unlabeled, i.e., 10 μM of 2-deoxyglucose,are added for 10 minutes at room temperature. The cells are washed threetimes with cold Phosphate Buffered Saline, “PBS”. The cells are lysedupon the addition of 150 μL/well of 0.2 N NaOH and subsequent incubationwith shaking for 20 minutes at room temperature. Samples are thentransferred to a scintillation vial to which is added 5 mL ofscintillation fluid. The vials are counted in a Beta-Scintillationcounter. Uptake in duplicate conditions, the difference being theabsence or presence of insulin, is determined with the followingequation: [(Insulin counts per minute “cpm”—Non-Specific cpm)/(NoInsulin cpm−Non-Specific cpm)]. Average responses fall within the limitsof about 5-fold and 3-fold that of controls for adipocytes and myotubes,respectively.

Differentiation of Cells

The cells are allowed to become fully confluent in a T-75 cm² flask. Themedium is removed and replaced with 25 mL of pre-differentiation mediumfor 48 hours. The cells are incubated at 37° C., in 5% CO₂, 85%humidity. After 48 hours, the pre-differentiation medium is removed andreplaced with 25 mL differentiation medium for 48 hours. The cells areagain incubated at 37° C., in 5% CO₂, 85% humidity. After 48 hours, themedium is removed and replaced with 30 mL post-differentiation medium.Post-differentiation medium is maintained for 14-20 days or untilcomplete differentiation is achieved. The medium is changed every 2-3days. Human adipocytes can be purchased from Zen-Bio, INC (# SA-1096).

Example 42 In Vitro Assay of [³H]-Thymidine Incorporation intoPancreatic Cell-Lines

It has recently been shown that GLP-1 induces differentiation of the ratpancreatic ductal epithelial cell-line ARIP in a time- anddose-dependent manner which is associated with an increase in IsletDuodenal Homeobox-1 (IDX-1) and insulin mRNA levels (Hui et al., 2001,Diabetes, 50(4): 785-96). The IDX-1 in turn increases mRNA levels of theGLP-1 receptor.

Cells Types Tested

RIN-M Cells:

These cells are available from the American Type Tissue CultureCollection (ATCC Cell Line Number CRL-2057). The RIN-M cell line wasderived from a radiation induced transplantable rat islet cell tumor.The line was established from a nude mouse xenograft of the tumor. Thecells produce and secrete islet polypeptide hormones, and produce L-dopadecarboxylase (a marker for cells having amine precursor uptake anddecarboxylation, or APUD, activity).

ARIP Cells:

These are pancreatic exocrine cells of epithelial morphology availablefrom the American Type Tissue Culture Collection (ATCC Cell Line NumberCRL-1674). See also, references: Jessop, N. W. and Hay, R. J.,“Characteristics of two rat pancreatic exocrine cell lines derived fromtransplantable tumors,” In Vitro 16: 212, (1980); Cockell, M. et al.,“Identification of a cell-specific DNA-binding activity that interactswith a transcriptional activator of genes expressed in the acinarpancreas,” Mol. Cell. Biol. 9: 2464-2476, (1989); Roux, E., et al. “Thecell-specific transcription factor PTF1 contains two different subunitsthat interact with the DNA” Genes Dev. 3: 1613-1624, (1989); and, Hui,H., et al., “Glucagon-like peptide 1 induces differentiation of isletduodenal homeobox-1-positive pancreatic ductal cells intoinsulin-secreting cells,” Diabetes 50: 785-796 (2001).

Preparation of Cells

The RIN-M cell-line is grown in RPMI 1640 medium (Hyclone, #SH300027.01)with 10% fetal bovine serum (HyClone, #SH30088.03) and is subculturedevery 6 to 8 days at a ratio of 1:3 to 1:6. The medium is changed every3 to 4 days.

The ARIP (ATCC #CRL-1674) cell-line is grown in Ham's F12K medium (ATCC,#30-2004) with 2 mM L-glutamine adjusted to contain 1.5 g/L sodiumbicarbonate and 10% fetal bovine serum. The ARIP cell-line issubcultured at a ratio of 1:3 to 1:6 twice per week. The medium ischanged every 3 to 4 days.

Assay Protocol

The cells are seeded at 4000 cells/well in 96-well plates and culturedfor 48 to 72 hours to 50% confluence. The cells are switched toserum-free media at 100 μL/well. After incubation for 48-72 hours, serumand/or the therapeutics of the subject invention (e.g., albumin fusionproteins of the invention and fragments and variants thereof) are addedto the well. Incubation persists for an additional 36 hours.[³H]-Thymidine (5-20 Ci/mmol) (Amersham Pharmacia, #TRK120) is dilutedto 1 microCuries/5 microliters. After the 36 hour incubation, 5microliters is added per well for a further 24 hours. The reaction isterminated by washing the cells gently with cold Phosphate-BufferedSaline, “PBS”, once. The cells are then fixed with 100 microliters of10% ice cold TCA for 15 min at 4° C. The PBS is removed and 200microliters of 0.2 N NaOH is added. The plates are incubated for 1 hourat room temperature with shaking. The solution is transferred to ascintillation vial and 5 mL of scintillation fluid compatible withaqueous solutions is added and mixed vigorously. The vials are countedin a beta scintillation counter. As negative control, only buffer isused. As a positive control fetal calf serum is used.

Example 43 Assaying for Glycosuria

Glycosuria (i.e., excess sugar in the urine), can be readily assayed toprovide an index of the disease state of diabetes mellitus. Excess urinein a patient sample as compared with a normal patient sample issymptomatic of IDDM and NIDDM. Efficacy of treatment of such a patienthaving IDDM and NIDDM is indicated by a resulting decrease in the amountof excess glucose in the urine. In a preferred embodiment for IDDM andNIDDM monitoring, urine samples from patients are assayed for thepresence of glucose using techniques known in the art. Glycosuria inhumans is defined by a urinary glucose concentration exceeding 100 mgper 100 ml. Excess sugar levels in those patients exhibiting glycosuriacan be measured even more precisely by obtaining blood samples andassaying serum glucose.

Example 44 Occurrence of Diabetes in NOD Mice

Female NOD (non-obese diabetic) mice are characterized by displayingIDDM with a course which is similar to that found in humans, althoughthe disease is more pronounced in female than male NOD mice.Hereinafter, unless otherwise stated, the term “NOD mouse” refers to afemale NOD mouse. NOD mice have a progressive destruction of beta cellswhich is caused by a chronic autoimmune disease. Thus, NOD mice beginlife with euglycemia, or normal blood glucose levels. By about 15 to 16weeks of age, however, NOD mice start becoming hyperglycemic, indicatingthe destruction of the majority of their pancreatic beta cells and thecorresponding inability of the pancreas to produce sufficient insulin.Thus, both the cause and the progression of the disease are similar tohuman IDDM patients.

In vivo assays of efficacy of the immunization regimens can be assessedin female NOD/LtJ mice (commercially available from The JacksonLaboratory, Bar Harbor, Me.). In the literature, it's reported that 80%of female mice develop diabetes by 24 weeks of age and onset ofinsulitis begins between 6-8 weeks age. NOD mice are inbred and highlyresponsive to a variety of immunoregulatory strategies. Adult NOD mice(6-8 weeks of age) have an average mass of 20-25 g.

These mice can be either untreated (control), treated with thetherapeutics of the subject invention (e.g., albumin fusion proteins ofthe invention and fragments and variants thereof), alone or incombination with other therapeutic compounds stated above. The effect ofthese various treatments on the progression of diabetes can be measuredas follows:

At 14 weeks of age, the female NOD mice can be phenotyped according toglucose tolerance. Glucose tolerance can be measured with theintraperitoneal glucose tolerance test (IPGTT). Briefly, blood is drawnfrom the paraorbital plexus at 0 minutes and 60 minutes after theintraperitoneal injection of glucose (1 g/kg body weight). Normaltolerance is defined as plasma glucose at 0 minutes of less than 144 mg%, or at 60 minutes of less than 160 mg %. Blood glucose levels aredetermined with a Glucometer Elite apparatus.

Based upon this phenotypic analysis, animals can be allocated to thedifferent experimental groups. In particular, animals with more elevatedblood glucose levels can be assigned to the impaired glucose tolerancegroup. The mice can be fed ad libitum and can be supplied with acidifiedwater (pH 2.3).

The glucose tolerant and intolerant mice can be further subdivided intocontrol, albumin fusion proteins of the subject invention, and albuminfusion proteins/therapeutic compounds combination groups. Mice in thecontrol group can receive an interperitoneal injection of vehicle daily,six times per week. Mice in the albumin fusion group can receive aninterperitoneal injection of the therapeutics of the subject invention(e.g., albumin fusion proteins of the invention and fragments andvariants thereof) in vehicle daily, six times per week. Mice in thealbumin fusion proteins/therapeutic compounds combination group canreceive both albumin fusion proteins and combinations of therapeuticcompounds as described above.

The level of urine glucose in the NOD mice can be determined on abi-weekly basis using Labstix (Bayer Diagnostics, Hampshire, England).Weight and fluid intake can also be determined on a bi-weekly basis. Theonset of diabetes is defined after the appearance of glucosuria on twoconsecutive determinations. After 10 weeks of treatment, an additionalIPGTT can be performed and animals can be sacrificed the following day.

Over the 10 week course of treatment, control animals in both theglucose tolerant and glucose intolerant groups develop diabetes at arate of 60% and 86%, respectively (see U.S. Pat. No. 5,866,546, Gross etal.). Thus, high rates of diabetes occur even in NOD mice which areinitially glucose tolerant if no intervention is made.

Results can be confirmed by the measurement of blood glucose levels inNOD mice, before and after treatment. Blood glucose levels are measuredas described above in both glucose tolerant and intolerant mice in allgroups described.

In an alternative embodiment, the therapeutics of the subject invention(e.g., specific fusions disclosed as SEQ ID NO:Y and fragments andvariants thereof) can be quantified using spectrometric analysis andappropriate protein quantities can be resuspended prior to injection in50 .mu·l phosphate buffered saline (PBS) per dose. Two injections, oneweek apart, can be administered subcutaneously under the dorsal skin ofeach mouse. Monitoring can be performed on two separate occasions priorto immunization and can be performed weekly throughout the treatment andcontinued thereafter. Urine can be tested for glucose every week(Keto-Diastix®; Miles Inc., Kankakee, Ill.) and glycosuric mice can bechecked for serum glucose (ExacTech®, MediSense, Inc., Waltham, Mass.).Diabetes is diagnosed when fasting glycemia is greater than 2.5 g/L.

Example 45 Histological Examination of NOD Mice

Histological examination of tissue samples from NOD mice can demonstratethe ability of the compositions of the present invention, and/or acombination of the compositions of the present invention with othertherapeutic agents for diabetes, to increase the relative concentrationof beta cells in the pancreas. The experimental method is as follows:

The mice from Example 44 can be sacrificed at the end of the treatmentperiod and tissue samples can be taken from the pancreas. The samplescan be fixed in 10% formalin in 0.9% saline and embedded in wax. Twosets of 5 serial 5 .mu·m sections can be cut for immunolabelling at acutting interval of 150 .mu·m. Sections can be immunolabelled forinsulin (guinea pig anti-insulin antisera dilution 1:1000, ICN ThamesU.K.) and glucagon (rabbit anti-pancreatic glucagon antisera dilution1:2000) and detected with peroxidase conjugated anti-guinea pig (Dako,High Wycombe, U.K.) or peroxidase conjugated anti-rabbit antisera(dilution 1:50, Dako).

The composition of the present invention may or may not have as strongan effect on the visible mass of beta cells as it does on the clinicalmanifestations of diabetes in glucose tolerant and glucose intolerantanimals.

Example 46 Pancreatic Beta-Cell Transplantation Combination Therapy

Transplantation is a common form of treatment of autoimmune disease,especially when the target self tissue has been severely damaged. Forexample, and not by way of limitation, pancreas transplantation andislet cell transplantation are common treatment options for IDDM (See,e.g., Stewart et al., Journal of Clinical Endocrinology & Metabolism 86(3): 984-988 (2001); Brunicardi, Transplant. Proc. 28: 2138-40 (1996);Kendall & Robertson, Diabetes Metab. 22: 157-163 (1996); Hamano et al.,Kobe J. Med. Sci. 42: 93-104 (1996); Larsen & Stratta, Diabetes Metab.22: 139-146 (1996); and Kinkhabwala, et al., Am. J. Surg. 171: 516-520(1996)). As with any transplantation method, transplantation therapiesfor autoimmune disease patients include treatments to minimize the riskof host rejection of the transplanted tissue. However, autoimmunedisease involves the additional, independent risk that the pre-existinghost autoimmune response which damaged the original self tissue willexert the same damaging effect on the transplanted tissue. Accordingly,the present invention encompasses methods and compositions for thetreatment of autoimmune pancreatic disease using the albumin fusionproteins of the subject invention in combination withimmunomodulators/immunosuppressants in individuals undergoingtransplantation therapy of the autoimmune disease.

In accordance with the invention, the albumin fusion-based compositionsand formulations described above, are administered to prevent and treatdamage to the transplanted organ, tissue, or cells resulting from thehost individual's autoimmune response initially directed against theoriginal self tissue. Administration may be carried out both prior andsubsequent to transplantation in 2 to 4 doses each one week apart.

The following immunomodulators/immunosuppressants including, but notlimited to, AI-401, CDP-571 (anti-TNF monoclonal antibody), CG-1088,Diamyd (diabetes vaccine), ICM3 (anti-ICAM-3 monoclonal antibody),linomide (Roquinimex), NBI-6024 (altered peptide ligand), TM-27, VX-740(HMR-3480), caspase 8 protease inhibitors, thalidomide, hOKT3gamma1(Ala-ala) (anti-CD3 monoclonal antibody), Oral Interferon-Alpha, orallactobacillus, and LymphoStat-B™ can be used together with the albuminfusion therapeutics of the subject invention in islet cell or pancreastransplantation.

Example 47 In Vivo Mouse Model of NIDDM

Male C57BL/6J mice from Jackson Laboratory (Bar Harbor, Me.) can beobtained at 3 weeks of age and fed on conventional chow or dietsenriched in either fat (35.5% wt/wt; Bioserv. Frenchtown, N.J.) orfructose (60% wt/wt; Harlan Teklad, Madison, Wis.). The regular chow iscomposed of 4.5% wt/wt fat, 23% wt/wt protein, 31.9% wt/wt starch, 3.7%wt/wt fructose, and 5.3% wt/wt fiber. The high-fat (lard) diet iscomposed of 35.5% wt/wt fat, 20% wt/wt protein, 36.4% wt/wt starch, 0.0%wt/wt fructose, and 0.1% wt/wt fiber. The high-fructose diet is composedof 5% wt/wt fat, 20% wt/wt protein, 0.0% wt/wt starch, 60% wt/wtfructose, and 9.4% wt/wt fiber. The mice may be housed no more than fiveper cage at 22°+/−3° C. temperature- and 50%+/−20% humidity-controlledroom with a 12-hour light (6 am to 6 pm)/dark cycle (Luo et al., 1998,Metabolism 47(6): 663-8, “Nongenetic mouse models ofnon-insulin-dependent diabetes mellitus”; Larsen et al., Diabetes50(11): 2530-9 (2001), “Systemic administration of the long-acting GLP-1derivative NN2211 induces lasting and reversible weight loss in bothnormal and obese rats”). After exposure to the respective diets for 3weeks, mice can be injected intraperitoneally with eitherstreptozotocin, “STZ” (Sigma, St. Louis, Mo.), at 100 mg/kg body weightor vehicle (0.05 mol/L citric acid, pH 4.5) and kept on the same dietfor the next 4 weeks. Under nonfasting conditions, blood is obtained 1,2, and 4 weeks post-STZ by nipping the distal part of the tail. Samplesare used to measure nonfasting plasma glucose and insulinconcentrations. Body weight and food intake are recorded weekly.

To directly determine the effect of the high-fat diet on the ability ofinsulin to stimulate glucose disposal, the experiments can be initiatedon three groups of mice, fat-fed, chow-fed injected with vehicle, andfat-fed injected with STZ at the end of the 7-week period describedabove. Mice can be fasted for 4 hours before the experiments. In thefirst series of experiments, mice can be anesthetized withmethoxyflurane (Pitman-Moor, Mundelein, Ill.) inhalation. Regularinsulin (Sigma) can be injected intravenously ([IV] 0.1 U/kg bodyweight) through a tail vein, and blood can be collected 3, 6, 9, 12, and15 minutes after the injection from a different tail vein. Plasmaglucose concentrations can be determined on these samples, and thehalf-life (t½) of glucose disappearance from plasma can be calculatedusing WinNonlin (Scientific Consulting, Apex, N.C.), apharmacokinetics/pharmacodynamics software program.

In the second series of experiments, mice can be anesthetized withintraperitoneal sodium pentobarbital (Sigma). The abdominal cavity isopened, and the main abdominal vein is exposed and catheterized with a24-gauge IV catheter (Johnson-Johnson Medical, Arlington, Tex.). Thecatheter is secured to muscle tissue adjacent to the abdominal vein, cuton the bottom of the syringe connection, and hooked to a prefilled PESOplastic tube, which in turn is connected to a syringe with infusionsolution. The abdominal cavity is then sutured closed. With thisapproach, there would be no blockage of backflow of the blood from thelower part of the body. Mice can be infused continuously with glucose(24.1 mg/kg/min) and insulin (10 mU/kg/min) at an infusion volume of 10μL/min. Retro-orbital blood samples (70 μL each) can be taken 90, 105,120, and 135 minutes after the start of infusion for measurement ofplasma glucose and insulin concentrations. The mean of these foursamples is used to estimate steady-state plasma glucose (SSPG) andinsulin (SSPI) concentrations for each animal.

Finally, experiments to evaluate the ability of the albumin fusionproteins, the therapeutic compositions of the instant application,either alone or in combination with any one or more of the therapeuticdrugs listed for the treatment of diabetes mellitus, to decrease plasmaglucose can be performed in the following two groups of “NIDDM” micemodels that are STZ-injected: (1) fat-fed C57BL/6J, and (2) fructose-fedC57BL/6J. Plasma glucose concentrations of the mice for these studiesmay range from 255 to 555 mg/dL. Mice are randomly assigned to treatmentwith either vehicle, albumin fusion therapeutics of the presentinvention either alone or in combination with any one or more of thetherapeutic drugs listed for the treatment of diabetes mellitus. A totalof three doses can be administered. Tail vein blood samples can be takenfor measurement of the plasma glucose concentration before the firstdose and 3 hours after the final dose.

Plasma glucose concentrations can be determined using the GlucoseDiagnostic Kit from Sigma (Sigma No. 315), an enzyme colorimetric assay.Plasma insulin levels can be determined using the Rat Insulin RIA Kitfrom Linco Research (#RI-13K; St. Charles, Mo.).

Example 48 In Vitro H4IIe-SEAP Reporter Assays Establishing Involvementin Insulin Action The Various H4IIe Reporters

H4IIe/rMEP-SEAP: The malic enzyme promoter isolated from rat (rMEP)contains a PPAR-gamma element which is in the insulin pathway. Thisreporter construct is stably transfected into the liver H4IIe cell-line.

H4IIe/SREBP-SEAP: The sterol regulatory element binding protein(SREBP-1c) is a transcription factor which acts on the promoters of anumber of insulin-responsive genes, for example, fatty acid synthetase(FAS), and which regulates expression of key genes in fatty acidmetabolism in fibroblasts, adipocytes, and hepatocytes. SREBP-1 c, alsoknown as the adipocyte determination and differentiation factor 1(ADD-1), is considered as the primary mediator of insulin effects ongene expression in adipose cells. It's activity is modulated by thelevels of insulin, sterols, and glucose. This reporter construct isstably transfected into the liver H4IIe cell-line.

H4IIe/FAS-SEAP: The fatty acid synthetase reporter constructs contain aminimal SREBP-responsive FAS promoter. This reporter construct is stablytransfected into the liver H4IIe cell-line.

H4IIe/PEPCK-SEAP: The phosphoenolpyruvate carboxykinase (PEPCK) promoteris the primary site of hormonal regulation of PEPCK gene transcriptionmodulating PEPCK activity. PEPCK catalyzes a committed and rate-limitingstep in hepatic gluconeogenesis and must therefore be carefullycontrolled to maintain blood glucose levels within normal limits. Thisreporter construct is stably transfected into the liver H4IIe cell-line.

These reporter constructs can also be stably transfected into 3T3-L1fibroblasts and L6 myoblasts. These stable cell-lines are thendifferentiated into 3T3-L1 adipocytes and L6 myotubes as previouslydescribed in Example 41. The differentiated cell-lines can then be usedin the SEAP assay described below.

Growth and Assay Medium

The growth medium comprises 10% Fetal Bovine Serum (FBS), 10% CalfSerum, 1% NEAA, 1× penicillin/streptomycin, and 0.75 mg/mL G418 (forH4IIe/rFAS-SEAP and H4IIe/SREBP-SEAP) or 0.50 mg/mL G418 (forH4IIe/rMEP-SEAP). For H4IIe/PEPCK-SEAP, the growth medium consists of10% FBS, 1% penicillin/streptomycin, 15 mM HEPES buffered saline, and0.50 mg/mL G418.

The assay medium consists of low glucose DMEM medium (LifeTechnologies), 1% NEAA, 1× penicillin/streptomycin for theH4IIe/rFAS-SEAP, H4IIe/SREBP-SEAP, H4IIe/rMEP-SEAP reporters. The assaymedium for H4IIe/PEPCK-SEAP reporter consists of 0.1% FBS, 1%penicillin/streptomycin, and 15 mM HEPES buffered saline.

Method

The 96-well plates are seeded at 75,000 cells/well in 100 μL/well ofgrowth medium until cells in log growth phase become adherent. Cells arestarved for 48 hours by replacing growth medium with assay medium, 200μL/well. (For H4IIe/PEPCK-SEAP cells, assay medium containing 0.5 μMdexamethasone is added at 100 μL/well and incubated for approximately 20hours). The assay medium is replaced thereafter with 100 μL/well offresh assay medium, and a 50 μL aliquot of cell supernatant obtainedfrom transfected cell-lines expressing the therapeutics of the subjectinvention (e.g., albumin fusion proteins of the invention and fragmentsand variants thereof) is added to the well. Supernatants from emptyvector transfected cell-lines are used as negative control. Addition of10 nM and/or 100 nM insulin to the wells is used as positive control.After 48 hours of incubation, the conditioned media are harvested andSEAP activity measured (Phospha-Light System protocol, Tropix #BP2500).Briefly, samples are diluted 1:4 in dilution buffer and incubated at 65°C. for 30 minutes to inactivate the endogenous non-placental form ofSEAP. An aliquot of 50 μL of the diluted samples is mixed with 50 μL ofSEAP Assay Buffer which contains a mixture of inhibitors active againstthe non-placental SEAP isoenzymes and is incubated for another 5minutes. An aliquot of 50 μL of CSPD chemiluminescent substrate which isdiluted 1:20 in Emerald luminescence enhancer is added to the mixtureand incubated for 15-20 minutes. Plates are read in a Dynex plateluminometer.

Example 49 Preparation of HA-Cytokine or HA-Growth Factor FusionProteins (Such as EPO, GMCSF, GCSF)

The cDNA for the cytokine or growth factor of interest, such as EPO, canbe isolated by a variety of means including from cDNA libraries, byRT-PCR and by PCR using a series of overlapping syntheticoligonucleotide primers, all using standard methods. The nucleotidesequences for all of these proteins are known and available, forinstance, in U.S. Pat. Nos. 4,703,008, 4,810,643 and 5,908,763. The cDNAcan be tailored at the 5′ and 3′ ends to generate restriction sites,such that oligonucleotide linkers can be used, for cloning of the cDNAinto a vector containing the cDNA for HA. This can be at the N orC-terminus with or without the use of a spacer sequence. EPO (or othercytokine) cDNA is cloned into a vector such as pPPC0005 (FIG. 2),pScCHSA, pScNHSA, or pC4:HSA from which the complete expression cassetteis then excised and inserted into the plasmid pSAC35 to allow theexpression of the albumin fusion protein in yeast. The albumin fusionprotein secreted from the yeast can then be collected and purified fromthe media and tested for its biological activity. For expression inmammalian cell lines, a similar procedure is adopted except that theexpression cassette used employs a mammalian promoter, leader sequenceand terminator (See Example 1). This expression cassette is then excisedand inserted into a plasmid suitable for the transfection of mammaliancell lines.

Example 50 Preparation of HA-IFN Fusion Proteins (Such as IFNα)

The cDNA for the interferon of interest such as IFNα can be isolated bya variety of means including but not exclusively, from cDNA libraries,by RT-PCR and by PCR using a series of overlapping syntheticoligonucleotide primers, all using standard methods. The nucleotidesequences for interferons, such as IFNα are known and available, forinstance, in U.S. Pat. Nos. 5,326,859 and 4,588,585, in EP 32 134, aswell as in public databases such as GenBank. The cDNA can be tailored atthe 5′ and 3′ ends to generate restriction sites, such thatoligonucleotide linkers can be used to clone the cDNA into a vectorcontaining the cDNA for HA. This can be at the N or C-terminus of the HAsequence, with or without the use of a spacer sequence. The IFNα (orother interferon) cDNA is cloned into a vector such as pPPC0005 (FIG.2), pScCHSA, pScNHSA, or pC4:HSA from which the complete expressioncassette is then excised and inserted into the plasmid pSAC35 to allowthe expression of the albumin fusion protein in yeast. The albuminfusion protein secreted from the yeast can then be collected andpurified from the media and tested for its biological activity. Forexpression in mammalian cell lines a similar procedure is adopted exceptthat the expression cassette used employs a mammalian promoter, leadersequence and terminator (See Example 1). This expression cassette isthen excised and inserted into a plasmid suitable for the transfectionof mammalian cell lines.

Maximum Protein Recovery from Vials

The albumin fusion proteins of the invention have a high degree ofstability even when they are packaged at low concentrations. Inaddition, in spite of the low protein concentration, good fusion-proteinrecovery is observed even when the aqueous solution includes no otherprotein added to minimize binding to the vial walls. The recovery ofvial-stored HA-IFN solutions was compared with a stock solution. 6 or 30μg/ml HA-IFN solutions were placed in vials and stored at 4° C. After 48or 72 hrs a volume originally equivalent to 10 ng of sample was removedand measured in an IFN sandwich ELISA. The estimated values werecompared to that of a high concentration stock solution. As shown, thereis essentially no loss of the sample in these vials, indicating thataddition of exogenous material such as albumin is not necessary toprevent sample loss to the wall of the vials

In Vivo Stability and Bioavailability of HA-α-IFN Fusions

To determine the in vivo stability and bioavailability of a HA-α-IFNfusion molecule, the purified fusion molecule (from yeast) wasadministered to monkeys. Pharmaceutical compositions formulated fromHA-α-IFN fusions may account for the extended serum half-life andbioavailability. Accordingly, pharmaceutical compositions may beformulated to contain lower dosages of alpha-interferon activitycompared to the native alpha-interferon molecule.

Pharmaceutical compositions containing HA-α-IFN fusions may be used totreat or prevent disease in patients with any disease or disease statethat can be modulated by the administration of α-IFN. Such diseasesinclude, but are not limited to, hairy cell leukemia, Kaposi's sarcoma,genital and anal warts, chronic hepatitis B, chronic non-A, non-Bhepatitis, in particular hepatitis C, hepatitis D, chronic myelogenousleukemia, renal cell carcinoma, bladder carcinoma, ovarian and cervicalcarcinoma, skin cancers, recurrent respirator papillomatosis,non-Hodgkin's and cutaneous T-cell lymphomas, melanoma, multiplemyeloma, AIDS, multiple sclerosis, gliobastoma, etc. (see InterferonAlpha, In: AHFS Drug Information, 1997.

Accordingly, the invention includes pharmaceutical compositionscontaining a HA-α-IFN fusion protein, polypeptide or peptide formulatedwith the proper dosage for human administration. The invention alsoincludes methods of treating patients in need of such treatmentcomprising at least the step of administering a pharmaceuticalcomposition containing at least one HA-α-IFN fusion protein, polypeptideor peptide.

Bifunctional HA-α-IFN Fusions

A HA-α-IFN expression vector may be modified to include an insertion forthe expression of bifunctional HA-α-IFN fusion proteins. For instance,the cDNA for a second protein of interest may be inserted in framedownstream of the “rHA-IFN” sequence after the double stop codon hasbeen removed or shifted downstream of the coding sequence.

In one version of a bifunctional HA-α-IFN fusion protein, an antibody orfragment against B-lymphocyte stimulator protein (GenBank Acc 4455139)or polypeptide may be fused to one end of the HA component of the fusionmolecule. This bifunctional protein is useful for modulating any immuneresponse generated by the α-IFN component of the fusion.

Example 51 Preparation of HA-Hormone Fusion Protein (Such as Insulin,LH, FSH)

The cDNA for the hormone of interest such as insulin can be isolated bya variety of means including but not exclusively, from cDNA libraries,by RT-PCR and by PCR using a series of overlapping syntheticoligonucleotide primers, all using standard methods. The nucleotidesequences for all of these proteins are known and available, forinstance, in public databases such as GenBank. The cDNA can be tailoredat the 5′ and 3′ ends to generate restriction sites, such thatoligonucleotide linkers can be used, for cloning of the cDNA into avector containing the cDNA for HA. This can be at the N or C-terminuswith or without the use of a spacer sequence. The hormone cDNA is clonedinto a vector such as pPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSAfrom which the complete expression cassette is then excised and insertedinto the plasmid pSAC35 to allow the expression of the albumin fusionprotein in yeast. The albumin fusion protein secreted from the yeast canthen be collected and purified from the media and tested for itsbiological activity. For expression in mammalian cell lines a similarprocedure is adopted except that the expression cassette used employs amammalian promoter, leader sequence and terminator (See Example 1). Thisexpression cassette is then excised and inserted into a plasmid suitablefor the transfection of mammalian cell lines.

Example 52 Preparation of HA-Soluble Receptor or HA-Binding ProteinFusion Protein Such as HA-TNF Receptor

The cDNA for the soluble receptor or binding protein of interest such asTNF receptor can be isolated by a variety of means including but notexclusively, from cDNA libraries, by RT-PCR and by PCR using a series ofoverlapping synthetic oligonucleotide primers, all using standardmethods. The nucleotide sequences for all of these proteins are knownand available, for instance, in GenBank. The cDNA can be tailored at the5′ and 3′ ends to generate restriction sites, such that oligonucleotidelinkers can be used, for cloning of the cDNA into a vector containingthe cDNA for HA. This can be at the N or C-terminus with or without theuse of a spacer sequence. The receptor cDNA is cloned into a vector suchas pPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSA from which thecomplete expression cassette is then excised and inserted into theplasmid pSAC35 to allow the expression of the albumin fusion protein inyeast. The albumin fusion protein secreted from the yeast can then becollected and purified from the media and tested for its biologicalactivity. For expression in mammalian cell lines a similar procedure isadopted except that the expression cassette used employs a mammalianpromoter, leader sequence and terminator (See Example 1). Thisexpression cassette is then excised and inserted into a plasmid suitablefor the transfection of mammalian cell lines.

Example 53 Preparation of HA-Growth Factors Such as HA-IGF-1 FusionProtein

The cDNA for the growth factor of interest such as IGF-1 can be isolatedby a variety of means including but not exclusively, from cDNAlibraries, by RT-PCR and by PCR using a series of overlapping syntheticoligonucleotide primers, all using standard methods (see GenBank Acc.No. NP_000609). The cDNA can be tailored at the 5′ and 3′ ends togenerate restriction sites, such that oligonucleotide linkers can beused, for cloning of the cDNA into a vector containing the cDNA for HA.This can be at the N or C-terminus with or without the use of a spacersequence. The growth factor cDNA is cloned into a vector such aspPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSA from which the completeexpression cassette is then excised and inserted into the plasmid pSAC35to allow the expression of the albumin fusion protein in yeast. Thealbumin fusion protein secreted from the yeast can then be collected andpurified from the media and tested for its biological activity. Forexpression in mammalian cell lines a similar procedure is adopted exceptthat the expression cassette used employs a mammalian promoter, leadersequence and terminator (See Example 1). This expression cassette isthen excised and inserted into a plasmid suitable for the transfectionof mammalian cell lines.

Example 54 Preparation of HA-Single Chain Antibody Fusion Proteins

Single chain antibodies are produced by several methods including butnot limited to: selection from phage libraries, cloning of the variableregion of a specific antibody by cloning the cDNA of the antibody andusing the flanking constant regions as the primer to clone the variableregion, or by synthesizing an oligonucleotide corresponding to thevariable region of any specific antibody. The cDNA can be tailored atthe 5′ and 3′ ends to generate restriction sites, such thatoligonucleotide linkers can be used, for cloning of the cDNA into avector containing the cDNA for HA. This can be at the N or C-terminuswith or without the use of a spacer sequence. The cell cDNA is clonedinto a vector such as pPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSAfrom which the complete expression cassette is then excised and insertedinto the plasmid pSAC35 to allow the expression of the albumin fusionprotein in yeast.

In fusion molecules of the invention, the V_(H) and V_(L) can be linkedby one of the following means or a combination thereof: a peptide linkerbetween the C-terminus of the V_(H) and the N-terminus of the V_(L); aKex2p protease cleavage site between the V_(H) and V_(L) such that thetwo are cleaved apart upon secretion and then self associate; andcysteine residues positioned such that the V_(H) and V_(L) can form adisulphide bond between them to link them together. An alternativeoption would be to place the V_(H) at the N-terminus of HA or an HAdomain fragment and the V_(L) at the C-terminus of the HA or HA domainfragment.

The albumin fusion protein secreted from the yeast can then be collectedand purified from the media and tested for its activity. For expressionin mammalian cell lines a similar procedure is adopted except that theexpression cassette used employs a mammalian promoter, leader sequenceand terminator (See Example 1). This expression cassette is then excisedand inserted into a plasmid suitable for the transfection of mammaliancell lines. The antibody produced in this manner can be purified frommedia and tested for its binding to its antigen using standardimmunochemical methods.

Example 55 Preparation of HA-Cell Adhesion Molecule Fusion Proteins

The cDNA for the cell adhesion molecule of interest can be isolated by avariety of means including but not exclusively, from cDNA libraries, byRT-PCR and by PCR using a series of overlapping syntheticoligonucleotide primers, all using standard methods. The nucleotidesequences for the known cell adhesion molecules are known and available,for instance, in GenBank. The cDNA can be tailored at the 5′ and 3′ endsto generate restriction sites, such that oligonucleotide linkers can beused, for cloning of the cDNA into a vector containing the cDNA for HA.This can be at the N or C-terminus with or without the use of a spacersequence. The cell adhesion molecule cDNA is cloned into a vector suchas pPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSA from which thecomplete expression cassette is then excised and inserted into theplasmid pSAC35 to allow the expression of the albumin fusion protein inyeast. The albumin fusion protein secreted from the yeast can then becollected and purified from the media and tested for its biologicalactivity. For expression in mammalian cell lines a similar procedure isadopted except that the expression cassette used employs a mammalianpromoter, leader sequence and terminator (See Example 1). Thisexpression cassette is then excised and inserted into a plasmid suitablefor the transfection of mammalian cell lines.

Example 56 Preparation of Inhibitory Factors and Peptides as HA FusionProteins (Such as HA-Antiviral, HA-Antibiotic, HA-Enzyme Inhibitor andHA-Anti-Allergic Proteins)

The cDNA for the peptide of interest such as an antibiotic peptide canbe isolated by a variety of means including but not exclusively, fromcDNA libraries, by RT-PCR and by PCR using a series of overlappingsynthetic oligonucleotide primers, all using standard methods. The cDNAcan be tailored at the 5′ and 3′ ends to generate restriction sites,such that oligonucleotide linkers can be used, for cloning of the cDNAinto a vector containing the cDNA for HA. This can be at the N orC-terminus with or without the use of a spacer sequence. The peptidecDNA is cloned into a vector such as pPPC0005 (FIG. 2), pScCHSA,pScNHSA, or pC4:HSA from which the complete expression cassette is thenexcised and inserted into the plasmid pSAC35 to allow the expression ofthe albumin fusion protein in yeast. The albumin fusion protein secretedfrom the yeast can then be collected and purified from the media andtested for its biological activity. For expression in mammalian celllines a similar procedure is adopted except that the expression cassetteused employs a mammalian promoter, leader sequence and terminator (SeeExample 1). This expression cassette is then excised and inserted into aplasmid suitable for the transfection of mammalian cell lines.

Example 57 Preparation of Targeted HA Fusion Proteins

The cDNA for the protein of interest can be isolated from cDNA libraryor can be made synthetically using several overlapping oligonucleotidesusing standard molecular biology methods. The appropriate nucleotidescan be engineered in the cDNA to form convenient restriction sites andalso allow the attachment of the protein cDNA to albumin cDNA similar tothe method described for hGH. Also a targeting protein or peptide cDNAsuch as single chain antibody or peptides, such as nuclear localizationsignals, that can direct proteins inside the cells can be fused to theother end of albumin. The protein of interest and the targeting peptideis cloned into a vector such as pPPC0005 (FIG. 2), pScCHSA, pScNHSA, orpC4:HSA which allows the fusion with albumin cDNA. In this manner bothN- and C-terminal end of albumin are fused to other proteins. The fusedcDNA is then excised from pPPC0005 and is inserted into a plasmid suchas pSAC35 to allow the expression of the albumin fusion protein inyeast. All the above procedures can be performed using standard methodsin molecular biology. The albumin fusion protein secreted from yeast canbe collected and purified from the media and tested for its biologicalactivity and its targeting activity using appropriate biochemical andbiological tests.

Example 58 Preparation of HA-Enzymes Fusions

The cDNA for the enzyme of interest can be isolated by a variety ofmeans including but not exclusively, from cDNA libraries, by RT-PCR andby PCR using a series of overlapping synthetic oligonucleotide primers,all using standard methods. The cDNA can be tailored at the 5′ and 3′ends to generate restriction sites, such that oligonucleotide linkerscan be used, for cloning of the cDNA into a vector containing the cDNAfor HA. This can be at the N or C-terminus with or without the use of aspacer sequence. The enzyme cDNA is cloned into a vector such aspPPC0005 (FIG. 2), pScCHSA, pScNHSA, or pC4:HSA from which the completeexpression cassette is then excised and inserted into the plasmid pSAC35to allow the expression of the albumin fusion protein in yeast. Thealbumin fusion protein secreted from the yeast can then be collected andpurified from the media and tested for its biological activity. Forexpression in mammalian cell lines a similar procedure is adopted exceptthat the expression cassette used employs a mammalian promoter, leadersequence and terminator (See Example 1). This expression cassette isthen excised and inserted into a plasmid suitable for the transfectionof mammalian cell lines.

Example 59 Bacterial Expression of an Albumin Fusion Protein

A polynucleotide encoding an albumin fusion protein of the presentinvention comprising a bacterial signal sequence is amplified using PCRoligonucleotide primers corresponding to the 5′ and 3′ ends of the DNAsequence, to synthesize insertion fragments. The primers used to amplifythe polynucleotide encoding insert should preferably contain restrictionsites, such as BamHI and XbaI, at the 5′ end of the primers in order toclone the amplified product into the expression vector. For example,BamHI and XbaI correspond to the restriction enzyme sites on thebacterial expression vector pQE-9. (Qiagen, Inc., Chatsworth, Calif.).This plasmid vector encodes antibiotic resistance (Ampr), a bacterialorigin of replication (ori), an IPTG-regulatable promoter/operator(P/O), a ribosome binding site (RBS), a 6-histidine tag (6-His), andrestriction enzyme cloning sites.

The pQE-9 vector is digested with BamHI and XbaI and the amplifiedfragment is ligated into the pQE-9 vector maintaining the reading frameinitiated at the bacterial RBS. The ligation mixture is then used totransform the E. coli strain M15/rep4 (Qiagen, Inc.) which containsmultiple copies of the plasmid pREP4, which expresses the lad repressorand also confers kanamycin resistance (Kan^(r)). Transformants areidentified by their ability to grow on LB plates andampicillin/kanamycin resistant colonies are selected. Plasmid DNA isisolated and confirmed by restriction analysis.

Clones containing the desired constructs are grown overnight (O/N) inliquid culture in LB media supplemented with both Amp (100 ug/ml) andKan (25 ug/ml). The 0/N culture is used to inoculate a large culture ata ratio of 1:100 to 1:250. The cells are grown to an optical density 600(O.D.⁶⁰⁰) of between 0.4 and 0.6. IPTG (Isopropyl-B-D-thiogalactopyranoside) is then added to a final concentration of 1 mM. IPTG inducesby inactivating the lad repressor, clearing the P/O leading to increasedgene expression.

Cells are grown for an extra 3 to 4 hours. Cells are then harvested bycentrifugation (20 mins at 6000×g). The cell pellet is solubilized inthe chaotropic agent 6 Molar Guanidine HCl or preferably in 8 M urea andconcentrations greater than 0.14 M 2-mercaptoethanol by stirring for 3-4hours at 4° C. (see, e.g., Burton et al., Eur. J. Biochem. 179:379-387(1989)). The cell debris is removed by centrifugation, and thesupernatant containing the polypeptide is loaded onto anickel-nitrilo-tri-acetic acid (“Ni-NTA”) affinity resin column(available from QIAGEN, Inc., supra). Proteins with a 6×His tag bind tothe Ni-NTA resin with high affinity and can be purified in a simpleone-step procedure (for details see: The QIAexpressionist (1995) QIAGEN,Inc., supra).

Briefly, the supernatant is loaded onto the column in 6 M guanidine-HCl,pH 8. The column is first washed with 10 volumes of 6 M guanidine-HCl,pH 8, then washed with 10 volumes of 6 M guanidine-HCl pH 6, and finallythe polypeptide is eluted with 6 M guanidine-HCl, pH 5.

The purified protein is then renatured by dialyzing it againstphosphate-buffered saline (PBS) or 50 mM Na-acetate, pH 6 buffer plus200 mM NaCl. Alternatively, the protein can be successfully refoldedwhile immobilized on the Ni-NTA column. Exemplary conditions are asfollows: renature using a linear 6M-1M urea gradient in 500 mM NaCl, 20%glycerol, 20 mM Tris/HCl pH 7.4, containing protease inhibitors. Therenaturation should be performed over a period of 1.5 hours or more.After renaturation the proteins are eluted by the addition of 250 mMimidazole. Imidazole is removed by a final dialyzing step against PBS or50 mM sodium acetate pH 6 buffer plus 200 mM NaCl. The purified proteinis stored at 4° C. or frozen at −80° C.

In addition to the above expression vector, the present inventionfurther includes an expression vector, called pHE4a (ATCC AccessionNumber 209645, deposited on Feb. 25, 1998) which contains phage operatorand promoter elements operatively linked to a polynucleotide encoding analbumin fusion protein of the present invention, called pHE4a. (ATCCAccession Number 209645, deposited on Feb. 25, 1998.) This vectorcontains: 1) a neomycinphosphotransferase gene as a selection marker, 2)an E. coli origin of replication, 3) a T5 phage promoter sequence, 4)two lac operator sequences, 5) a Shine-Delgarno sequence, and 6) thelactose operon repressor gene (lacIq). The origin of replication (oriC)is derived from pUC19 (LTI, Gaithersburg, Md.). The promoter andoperator sequences are made synthetically.

DNA can be inserted into the pHE4a by restricting the vector with NdeIand XbaI, BamHI, XhoI, or Asp718, running the restricted product on agel, and isolating the larger fragment (the stuffer fragment should beabout 310 base pairs). The DNA insert is generated according to PCRprotocols described herein or otherwise known in the art, using PCRprimers having restriction sites for NdeI (5′ primer) and XbaI, BamHI,XhoI, or Asp718 (3′ primer). The PCR insert is gel purified andrestricted with compatible enzymes. The insert and vector are ligatedaccording to standard protocols.

The engineered vector may be substituted in the above protocol toexpress protein in a bacterial system.

Example 60 Expression of an Albumin Fusion Protein in Mammalian Cells

The albumin fusion proteins of the present invention can be expressed ina mammalian cell. A typical mammalian expression vector contains apromoter element, which mediates the initiation of transcription ofmRNA, a protein coding sequence, and signals required for thetermination of transcription and polyadenylation of the transcript.Additional elements include enhancers, Kozak sequences and interveningsequences flanked by donor and acceptor sites for RNA splicing. Highlyefficient transcription is achieved with the early and late promotersfrom SV40, the long terminal repeats (LTRs) from Retroviruses, e.g.,RSV, HTLVI, HIVI and the early promoter of the cytomegalovirus (CMV).However, cellular elements can also be used (e.g., the human actinpromoter).

Suitable expression vectors for use in practicing the present inventioninclude, for example, vectors such as, pSVL and pMSG (Pharmacia,Uppsala, Sweden), pRSVcat (ATCC 37152), pSV2dhfr (ATCC 37146), pBC12MI(ATCC 67109), pCMVSport 2.0, and pCMVSport 3.0. Mammalian host cellsthat could be used include, but are not limited to, human Hela, 293, H9and Jurkat cells, mouse NIH3T3 and C127 cells, Cos 1, Cos 7 and CV1,quail QC1-3 cells, mouse L cells and Chinese hamster ovary (CHO) cells.

Alternatively, the albumin fusion protein can be expressed in stablecell lines containing the polynucleotide encoding the albumin fusionprotein integrated into a chromosome. The co-transfection with aselectable marker such as DHFR, gpt, neomycin, or hygromycin allows theidentification and isolation of the transfected cells.

The transfected polynucleotide encoding the fusion protein can also beamplified to express large amounts of the encoded fusion protein. TheDHFR (dihydrofolate reductase) marker is useful in developing cell linesthat carry several hundred or even several thousand copies of the geneof interest. (See, e.g., Alt et al., J. Biol. Chem. 253:1357-1370(1978); Hamlin et al., Biochem. et Biophys. Acta, 1097:107-143 (1990);Page et al., Biotechnology 9:64-68 (1991)). Another useful selectionmarker is the enzyme glutamine synthase (GS) (Murphy et al., Biochem J.227:277-279 (1991); Bebbington et al., Bio/Technology 10:169-175 (1992).Using these markers, the mammalian cells are grown in selective mediumand the cells with the highest resistance are selected. These cell linescontain the amplified gene(s) integrated into a chromosome. Chinesehamster ovary (CHO) and NSO cells are often used for the production ofproteins.

Derivatives of the plasmid pSV2-dhfr (ATCC Accession No. 37146), theexpression vectors pC4 (ATCC Accession No. 209646) and pC6 (ATCCAccession No. 209647) contain the strong promoter (LTR) of the RousSarcoma Virus (Cullen et al., Molecular and Cellular Biology, 438-447(March, 1985)) plus a fragment of the CMV-enhancer (Boshart et al., Cell41:521-530 (1985)). Multiple cloning sites, e.g., with the restrictionenzyme cleavage sites BamHI, XbaI and Asp718, facilitate the cloning ofthe gene of interest. The vectors also contain the 3′ intron, thepolyadenylation and termination signal of the rat preproinsulin gene,and the mouse DHFR gene under control of the SV40 early promoter.

Specifically, the plasmid pC6, for example, is digested with appropriaterestriction enzymes and then dephosphorylated using calf intestinalphosphates by procedures known in the art. The vector is then isolatedfrom a 1% agarose gel.

A polynucleotide encoding an albumin fusion protein of the presentinvention is generated using techniques known in the art and thispolynucleotide is amplified using PCR technology known in the art. If anaturally occurring signal sequence is used to produce the fusionprotein of the present invention, the vector does not need a secondsignal peptide. Alternatively, if a naturally occurring signal sequenceis not used, the vector can be modified to include a heterologous signalsequence. (See, e.g., International Publication No. WO 96/34891.)

The amplified fragment encoding the fusion protein of the invention isisolated from a 1% agarose gel using a commercially available kit(“Geneclean,” BIO 101 Inc., La Jolla, Ca.). The fragment then isdigested with appropriate restriction enzymes and again purified on a 1%agarose gel.

The amplified fragment encoding the albumin fusion protein of theinvention is then digested with the same restriction enzyme and purifiedon a 1% agarose gel. The isolated fragment and the dephosphorylatedvector are then ligated with T4 DNA ligase. E. coli HB101 or XL-1 Bluecells are then transformed and bacteria are identified that contain thefragment inserted into plasmid pC6 using, for instance, restrictionenzyme analysis.

Chinese hamster ovary cells lacking an active DHFR gene is used fortransfection. Five μg of the expression plasmid pC6 or pC4 iscotransfected with 0.5 μg of the plasmid pSVneo using lipofectin(Felgner et al., supra). The plasmid pSV2-neo contains a dominantselectable marker, the neo gene from Tn5 encoding an enzyme that confersresistance to a group of antibiotics including G418. The cells areseeded in alpha minus MEM supplemented with 1 mg/ml G418. After 2 days,the cells are trypsinized and seeded in hybridoma cloning plates(Greiner, Germany) in alpha minus MEM supplemented with 10, 25, or 50ng/ml of methotrexate plus 1 mg/ml G418. After about 10-14 days singleclones are trypsinized and then seeded in 6-well petri dishes or 10 mlflasks using different concentrations of methotrexate (50 nM, 100 nM,200 nM, 400 nM, 800 nM). Clones growing at the highest concentrations ofmethotrexate are then transferred to new 6-well plates containing evenhigher concentrations of methotrexate (1 μM, 2 μM, 5 μM, 10 mM, 20 mM).The same procedure is repeated until clones are obtained which grow at aconcentration of 100-200 μM. Expression of the desired fusion protein isanalyzed, for instance, by SDS-PAGE and Western blot or by reversedphase HPLC analysis.

Example 61 Multifusion Fusions

The albumin fusion proteins (e.g., containing a Therapeutic protein (orfragment or variant thereof) fused to albumin (or a fragment or variantthereof)) may additionally be fused to other proteins to generate“multifusion proteins”. These multifusion proteins can be used for avariety of applications. For example, fusion of the albumin fusionproteins of the invention to His-tag, HA-tag, protein A, IgG domains,and maltose binding protein facilitates purification. (See e.g., EP A394,827; Traunecker et al., Nature 331:84-86 (1988)). Nuclearlocalization signals fused to the polypeptides of the present inventioncan target the protein to a specific subcellular localization, whilecovalent heterodimer or homodimers can increase or decrease the activityof an albumin fusion protein. Furthermore, the fusion of additionalprotein sequences to the albumin fusion proteins of the invention mayfurther increase the solubility and/or stability of the fusion protein.The fusion proteins described above can be made using or routinelymodifying techniques known in the art and/or by modifying the followingprotocol, which outlines the fusion of a polypeptide to an IgG molecule.

Briefly, the human Fc portion of the IgG molecule can be PCR amplified,using primers that span the 5′ and 3′ ends of the sequence describedbelow. These primers also should have convenient restriction enzymesites that will facilitate cloning into an expression vector, preferablya mammalian or yeast expression vector.

For example, if pC4 (ATCC Accession No. 209646) is used, the human Fcportion can be ligated into the BamHI cloning site. Note that the 3′BamHI site should be destroyed. Next, the vector containing the human Fcportion is re-restricted with BamHI, linearizing the vector, and apolynucleotide encoding an albumin fusion protein of the presentinvention (generated and isolated using techniques known in the art), isligated into this BamHI site. Note that the polynucleotide encoding thefusion protein of the invention is cloned without a stop codon,otherwise a Fc containing fusion protein will not be produced.

If the naturally occurring signal sequence is used to produce thealbumin fusion protein of the present invention, pC4 does not need asecond signal peptide. Alternatively, if the naturally occurring signalsequence is not used, the vector can be modified to include aheterologous signal sequence. (See, e.g., International Publication No.WO 96/34891.)

Human IgG Fc region: (SEQ ID NO: 1112)GGGATCCGGAGCCCAAATCTTCTGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAATTCGAGGGTGCACCGTCAGTCTTCCTCTTCCCCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACTCCTGAGGTCACATGCGTGGTGGTGGACGTAAGCCACGAAGACCCTGAGGTCAAGTTCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCAACCCCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCATCCCGGGATGAGCTGACCAAGAACCAGGTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATCCAAGCGACATCGCCGTGGAGTGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTACAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTAAATGAGTGCGACGGCCGCGACTCTAGAGGAT

Example 62 Production of an Antibody from an Albumin Fusion ProteinHybridoma Technology

Antibodies that bind the albumin fusion proteins of the presentinvention and portions of the albumin fusion proteins of the presentinvention (e.g., the Therapeutic protein portion or albumin portion ofthe fusion protein) can be prepared by a variety of methods. (See,Current Protocols, Chapter 2.) As one example of such methods, apreparation of an albumin fusion protein of the invention or a portionof an albumin fusion protein of the invention is prepared and purifiedto render it substantially free of natural contaminants. Such apreparation is then introduced into an animal in order to producepolyclonal antisera of greater specific activity.

Monoclonal antibodies specific for an albumin fusion protein of theinvention, or a portion of an albumin fusion protein of the invention,are prepared using hybridoma technology (Kohler et al., Nature 256:495(1975); Kohler et al., Eur. J. Immunol. 6:511 (1976); Kohler et al.,Eur. J. Immunol. 6:292 (1976); Hammerling et al., in: MonoclonalAntibodies and T-Cell Hybridomas, Elsevier, N.Y., pp. 563-681 (1981)).In general, an animal (preferably a mouse) is immunized with an albuminfusion protein of the invention, or a portion of an albumin fusionprotein of the invention. The splenocytes of such mice are extracted andfused with a suitable myeloma cell line. Any suitable myeloma cell linemay be employed in accordance with the present invention; however, it ispreferable to employ the parent myeloma cell line (SP20), available fromthe ATCC. After fusion, the resulting hybridoma cells are selectivelymaintained in HAT medium, and then cloned by limiting dilution asdescribed by Wands et al. (Gastroenterology 80:225-232 (1981)). Thehybridoma cells obtained through such a selection are then assayed toidentify clones which secrete antibodies capable of binding an albuminfusion protein of the invention, or a portion of an albumin fusionprotein of the invention.

Alternatively, additional antibodies capable of binding to an albuminfusion protein of the invention, or a portion of an albumin fusionprotein of the invention can be produced in a two-step procedure usinganti-idiotypic antibodies. Such a method makes use of the fact thatantibodies are themselves antigens, and therefore, it is possible toobtain an antibody which binds to a second antibody. In accordance withthis method, protein specific antibodies are used to immunize an animal,preferably a mouse. The splenocytes of such an animal are then used toproduce hybridoma cells, and the hybridoma cells are screened toidentify clones which produce an antibody whose ability to bind to thean albumin fusion protein of the invention (or portion of an albuminfusion protein of the invention)-specific antibody can be blocked by thefusion protein of the invention, or a portion of an albumin fusionprotein of the invention. Such antibodies comprise anti-idiotypicantibodies to the fusion protein of the invention (or portion of analbumin fusion protein of the invention)-specific antibody and are usedto immunize an animal to induce formation of further fusion protein ofthe invention (or portion of an albumin fusion protein of theinvention)-specific antibodies.

For in vivo use of antibodies in humans, an antibody is “humanized”.Such antibodies can be produced using genetic constructs derived fromhybridoma cells producing the monoclonal antibodies described above.Methods for producing chimeric and humanized antibodies are known in theart and are discussed herein. (See, for review, Morrison, Science229:1202 (1985); Oi et al., BioTechniques 4:214 (1986); Cabilly et al.,U.S. Pat. No. 4,816,567; Taniguchi et al., EP 171496; Morrison et al.,EP 173494; Neuberger et al., WO 8601533; Robinson et al., InternationalPublication No. WO 8702671; Boulianne et al., Nature 312:643 (1984);Neuberger et al., Nature 314:268 (1985)).

Isolation of Antibody Fragments Directed Against an Albumin FusionProtein of the Invention, or a Portion of an Albumin Fusion Protein ofthe Invention from a Library of scFvs.

Naturally occurring V-genes isolated from human PBLs are constructedinto a library of antibody fragments which contain reactivities againstan albumin fusion protein of the invention, or a portion of an albuminfusion protein of the invention, to which the donor may or may not havebeen exposed (see e.g., U.S. Pat. No. 5,885,793 incorporated herein byreference in its entirety).

Rescue of the Library.

A library of scFvs is constructed from the RNA of human PBLs asdescribed in International Publication No. WO 92/01047. To rescue phagedisplaying antibody fragments, approximately 10⁹ E. coli harboring thephagemid are used to inoculate 50 ml of 2×TY containing 1% glucose and100 μg/ml of ampicillin (2×TY-AMP-GLU) and grown to an O.D. of 0.8 withshaking. Five ml of this culture is used to inoculate 50 ml of2×TY-AMP-GLU, 2×108 TU of delta gene 3 helper (M13 delta gene III, seeInternational Publication No. WO 92/01047) are added and the cultureincubated at 37° C. for 45 minutes without shaking and then at 37° C.for 45 minutes with shaking. The culture is centrifuged at 4000 r.p.m.for 10 min. and the pellet resuspended in 2 liters of 2×TY containing100 μg/ml ampicillin and 50 ug/ml kanamycin and grown overnight. Phageare prepared as described in International Publication No. WO 92/01047.

M13 delta gene III is prepared as follows: M13 delta gene III helperphage does not encode gene III protein, hence the phage(mid) displayingantibody fragments have a greater avidity of binding to antigen.Infectious M13 delta gene III particles are made by growing the helperphage in cells harboring a pUC19 derivative supplying the wild type geneIII protein during phage morphogenesis. The culture is incubated for 1hour at 37° C. without shaking and then for a further hour at 37° C.with shaking. Cells are spun down (IEC-Centra 8,400 r.p.m. for 10 min),resuspended in 300 ml 2×TY broth containing 100 μg ampicillin/ml and 25μg kanamycin/ml (2×TY-AMP-KAN) and grown overnight, shaking at 37° C.Phage particles are purified and concentrated from the culture medium bytwo PEG-precipitations (Sambrook et al., 1990), resuspended in 2 ml PBSand passed through a 0.45 μm filter (Minisart NML; Sartorius) to give afinal concentration of approximately 10¹³ transducing units/ml(ampicillin-resistant clones).

Panning of the Library.

Immunotubes (Nunc) are coated overnight in PBS with 4 ml of either 100μg/ml or 10 μg/ml of an albumin fusion protein of the invention, or aportion of an albumin fusion protein of the invention. Tubes are blockedwith 2% Marvel-PBS for 2 hours at 37° C. and then washed 3 times in PBS.Approximately 10¹³ TU of phage is applied to the tube and incubated for30 minutes at room temperature tumbling on an over and under turntableand then left to stand for another 1.5 hours. Tubes are washed 10 timeswith PBS 0.1% Tween-20 and 10 times with PBS. Phage are eluted by adding1 ml of 100 mM triethylamine and rotating 15 minutes on an under andover turntable after which the solution is immediately neutralized with0.5 ml of 1.0M Tris-HCl, pH 7.4. Phage are then used to infect 10 ml ofmid-log E. coli TG1 by incubating eluted phage with bacteria for 30minutes at 37° C. The E. coli are then plated on TYE plates containing1% glucose and 100 μg/ml ampicillin. The resulting bacterial library isthen rescued with delta gene 3 helper phage as described above toprepare phage for a subsequent round of selection. This process is thenrepeated for a total of 4 rounds of affinity purification withtube-washing increased to 20 times with PBS, 0.1% Tween-20 and 20 timeswith PBS for rounds 3 and 4.

Characterization of Binders.

Eluted phage from the 3rd and 4th rounds of selection are used to infectE. coli HB 2151 and soluble scFv is produced (Marks, et al., 1991) fromsingle colonies for assay. ELISAs are performed with microtitre platescoated with either 10 pg/ml of an albumin fusion protein of theinvention, or a portion of an albumin fusion protein of the invention,in 50 mM bicarbonate pH 9.6. Clones positive in ELISA are furthercharacterized by PCR fingerprinting (see, e.g., InternationalPublication No. WO 92/01047) and then by sequencing. These ELISApositive clones may also be further characterized by techniques known inthe art, such as, for example, epitope mapping, binding affinity,receptor signal transduction, ability to block or competitively inhibitantibody/antigen binding, and competitive agonistic or antagonisticactivity.

Example 63 Method of Treatment Using Gene Therapy-Ex Vivo

One method of gene therapy transplants fibroblasts, which are capable ofexpressing an albumin fusion protein of the present invention, onto apatient. Generally, fibroblasts are obtained from a subject by skinbiopsy. The resulting tissue is placed in tissue-culture medium andseparated into small pieces. Small chunks of the tissue are placed on awet surface of a tissue culture flask, approximately ten pieces areplaced in each flask. The flask is turned upside down, closed tight andleft at room temperature over night. After 24 hours at room temperature,the flask is inverted and the chunks of tissue remain fixed to thebottom of the flask and fresh media (e.g., Ham's F12 media, with 10%FBS, penicillin and streptomycin) is added. The flasks are thenincubated at 37 degree C. for approximately one week.

At this time, fresh media is added and subsequently changed everyseveral days. After an additional two weeks in culture, a monolayer offibroblasts emerge. The monolayer is trypsinized and scaled into largerflasks.

pMV-7 (Kirschmeier, P. T. et al., DNA, 7:219-25 (1988)), flanked by thelong terminal repeats of the Moloney murine sarcoma virus, is digestedwith EcoRI and HindIII and subsequently treated with calf intestinalphosphatase. The linear vector is fractionated on agarose gel andpurified, using glass beads.

Polynucleotides encoding an albumin fusion protein of the invention canbe generated using techniques known in the art amplified using PCRprimers which correspond to the 5′ and 3′ end sequences and optionallyhaving appropriate restriction sites and initiation/stop codons, ifnecessary. Preferably, the 5′ primer contains an EcoRI site and the 3′primer includes a HindIII site. Equal quantities of the Moloney murinesarcoma virus linear backbone and the amplified EcoRI and HindIIIfragment are added together, in the presence of T4 DNA ligase. Theresulting mixture is maintained under conditions appropriate forligation of the two fragments. The ligation mixture is then used totransform bacteria HB101, which are then plated onto agar containingkanamycin for the purpose of confirming that the vector has the gene ofinterest properly inserted.

The amphotropic pA317 or GP+am12 packaging cells are grown in tissueculture to confluent density in Dulbecco's Modified Eagles Medium (DMEM)with 10% calf serum (CS), penicillin and streptomycin. The MSV vectorcontaining the gene is then added to the media and the packaging cellstransduced with the vector. The packaging cells now produce infectiousviral particles containing the gene (the packaging cells are nowreferred to as producer cells).

Fresh media is added to the transduced producer cells, and subsequently,the media is harvested from a 10 cm plate of confluent producer cells.The spent media, containing the infectious viral particles, is filteredthrough a millipore filter to remove detached producer cells and thismedia is then used to infect fibroblast cells. Media is removed from asub-confluent plate of fibroblasts and quickly replaced with the mediafrom the producer cells. This media is removed and replaced with freshmedia. If the titer of virus is high, then virtually all fibroblastswill be infected and no selection is required. If the titer is very low,then it is necessary to use a retroviral vector that has a selectablemarker, such as neo or his. Once the fibroblasts have been efficientlyinfected, the fibroblasts are analyzed to determine whether the albuminfusion protein is produced.

The engineered fibroblasts are then transplanted onto the host, eitheralone or after having been grown to confluence on cytodex 3 microcarrierbeads.

Example 64 Method of Treatment Using Gene Therapy—In Vivo

Another aspect of the present invention is using in vivo gene therapymethods to treat disorders, diseases and conditions. The gene therapymethod relates to the introduction of naked nucleic acid (DNA, RNA, andantisense DNA or RNA) sequences encoding an albumin fusion protein ofthe invention into an animal. Polynucleotides encoding albumin fusionproteins of the present invention may be operatively linked to (i.e.,associated with) a promoter or any other genetic elements necessary forthe expression of the polypeptide by the target tissue. Such genetherapy and delivery techniques and methods are known in the art, see,for example, WO90/11092, WO98/11779; U.S. Pat. Nos. 5,693,622,5,705,151, 5,580,859; Tabata et al., Cardiovasc. Res. 35(3):470-479(1997); Chao et al., Pharmacol. Res. 35(6):517-522 (1997); Wolff,Neuromuscul. Disord. 7(5):314-318 (1997); Schwartz et al., Gene Ther.3(5):405-411 (1996); Tsurumi et al., Circulation 94(12):3281-3290 (1996)(incorporated herein by reference).

The polynucleotide constructs may be delivered by any method thatdelivers injectable materials to the cells of an animal, such as,injection into the interstitial space of tissues (heart, muscle, skin,lung, liver, intestine and the like). The polynucleotide constructs canbe delivered in a pharmaceutically acceptable liquid or aqueous carrier.

The term “naked” polynucleotide, DNA or RNA, refers to sequences thatare free from any delivery vehicle that acts to assist, promote, orfacilitate entry into the cell, including viral sequences, viralparticles, liposome formulations, lipofectin or precipitating agents andthe like. However, polynucleotides encoding albumin fusion proteins ofthe present invention may also be delivered in liposome formulations(such as those taught in Felgner P. L. et al. (1995) Ann. NY Acad. Sci.772:126-139 and Abdallah B. et al. (1995) Biol. Cell 85(1):1-7) whichcan be prepared by methods well known to those skilled in the art.

The polynucleotide vector constructs used in the gene therapy method arepreferably constructs that will not integrate into the host genome norwill they contain sequences that allow for replication. Any strongpromoter known to those skilled in the art can be used for driving theexpression of DNA. Unlike other gene therapy techniques, one majoradvantage of introducing naked nucleic acid sequences into target cellsis the transitory nature of the polynucleotide synthesis in the cells.Studies have shown that non-replicating DNA sequences can be introducedinto cells to provide production of the desired polypeptide for periodsof up to six months.

The polynucleotide construct can be delivered to the interstitial spaceof tissues within an animal, including muscle, skin, brain, lung, liver,spleen, bone marrow, thymus, heart, lymph, blood, bone, cartilage,pancreas, kidney, gall bladder, stomach, intestine, testis, ovary,uterus, rectum, nervous system, eye, gland, and connective tissue.Interstitial space of the tissues comprises the intercellular fluid,mucopolysaccharide matrix among the reticular fibers of organ tissues,elastic fibers in the walls of vessels or chambers, collagen fibers offibrous tissues, or that same matrix within connective tissueensheathing muscle cells or in the lacunae of bone. It is similarly thespace occupied by the plasma of the circulation and the lymph fluid ofthe lymphatic channels. Delivery to the interstitial space of muscletissue is preferred for the reasons discussed below. They may beconveniently delivered by injection into the tissues comprising thesecells. They are preferably delivered to and expressed in persistent,non-dividing cells which are differentiated, although delivery andexpression may be achieved in non-differentiated or less completelydifferentiated cells, such as, for example, stem cells of blood or skinfibroblasts. In vivo muscle cells are particularly competent in theirability to take up and express polynucleotides.

For the naked polynucleotide injection, an effective dosage amount ofDNA or RNA will be in the range of from about 0.05 g/kg body weight toabout 50 mg/kg body weight. Preferably the dosage will be from about0.005 mg/kg to about 20 mg/kg and more preferably from about 0.05 mg/kgto about 5 mg/kg. Of course, as the artisan of ordinary skill willappreciate, this dosage will vary according to the tissue site ofinjection. The appropriate and effective dosage of nucleic acid sequencecan readily be determined by those of ordinary skill in the art and maydepend on the condition being treated and the route of administration.The preferred route of administration is by the parenteral route ofinjection into the interstitial space of tissues. However, otherparenteral routes may also be used, such as, inhalation of an aerosolformulation particularly for delivery to lungs or bronchial tissues,throat or mucous membranes of the nose. In addition, nakedpolynucleotide constructs can be delivered to arteries duringangioplasty by the catheter used in the procedure.

The dose response effects of injected polynucleotide in muscle in vivois determined as follows. Suitable template DNA for production of mRNAcoding for polypeptide of the present invention is prepared inaccordance with a standard recombinant DNA methodology. The templateDNA, which may be either circular or linear, is either used as naked DNAor complexed with liposomes. The quadriceps muscles of mice are theninjected with various amounts of the template DNA.

Five to six week old female and male Balb/C mice are anesthetized byintraperitoneal injection with 0.3 ml of 2.5% Avertin. A 1.5 cm incisionis made on the anterior thigh, and the quadriceps muscle is directlyvisualized. The template DNA is injected in 0.1 ml of carrier in a 1 ccsyringe through a 27 gauge needle over one minute, approximately 0.5 cmfrom the distal insertion site of the muscle into the knee and about 0.2cm deep. A suture is placed over the injection site for futurelocalization, and the skin is closed with stainless steel clips.

After an appropriate incubation time (e.g., 7 days) muscle extracts areprepared by excising the entire quadriceps. Every fifth 15 umcross-section of the individual quadriceps muscles is histochemicallystained for protein expression. A time course for fusion proteinexpression may be done in a similar fashion except that quadriceps fromdifferent mice are harvested at different times. Persistence of DNA inmuscle following injection may be determined by Southern blot analysisafter preparing total cellular DNA and HIRT supernatants from injectedand control mice. The results of the above experimentation in mice canbe used to extrapolate proper dosages and other treatment parameters inhumans and other animals using naked DNA.

Example 65 Transgenic Animals

The albumin fusion proteins of the invention can also be expressed intransgenic animals. Animals of any species, including, but not limitedto, mice, rats, rabbits, hamsters, guinea pigs, pigs, micro-pigs, goats,sheep, cows and non-human primates, e.g., baboons, monkeys, andchimpanzees may be used to generate transgenic animals. In a specificembodiment, techniques described herein or otherwise known in the art,are used to express fusion proteins of the invention in humans, as partof a gene therapy protocol.

Any technique known in the art may be used to introduce thepolynucleotides encoding the albumin fusion proteins of the inventioninto animals to produce the founder lines of transgenic animals. Suchtechniques include, but are not limited to, pronuclear microinjection(Paterson et al., Appl. Microbiol. Biotechnol. 40:691-698 (1994); Carveret al., Biotechnology (NY) 11:1263-1270 (1993); Wright et al.,Biotechnology (NY) 9:830-834 (1991); and Hoppe et al., U.S. Pat. No.4,873,191 (1989)); retrovirus mediated gene transfer into germ lines(Van der Putten et al., Proc. Natl. Acad. Sci., USA 82:6148-6152(1985)), blastocysts or embryos; gene targeting in embryonic stem cells(Thompson et al., Cell 56:313-321 (1989)); electroporation of cells orembryos (Lo, 1983, Mol Cell. Biol. 3:1803-1814 (1983)); introduction ofthe polynucleotides of the invention using a gene gun (see, e.g., Ulmeret al., Science 259:1745 (1993); introducing nucleic acid constructsinto embryonic pleuripotent stem cells and transferring the stem cellsback into the blastocyst; and sperm-mediated gene transfer (Lavitrano etal., Cell 57:717-723 (1989); etc. For a review of such techniques, seeGordon, “Transgenic Animals,” Intl. Rev. Cytol. 115:171-229 (1989),which is incorporated by reference herein in its entirety.

Any technique known in the art may be used to produce transgenic clonescontaining polynucleotides encoding albumin fusion proteins of theinvention, for example, nuclear transfer into enucleated oocytes ofnuclei from cultured embryonic, fetal, or adult cells induced toquiescence (Campell et al., Nature 380:64-66 (1996); Wilmut et al.,Nature 385:810-813 (1997)).

The present invention provides for transgenic animals that carry thepolynucleotides encoding the albumin fusion proteins of the invention inall their cells, as well as animals which carry these polynucleotides insome, but not all their cells, i.e., mosaic animals or chimeric. Thetransgene may be integrated as a single transgene or as multiple copiessuch as in concatamers, e.g., head-to-head tandems or head-to-tailtandems. The transgene may also be selectively introduced into andactivated in a particular cell type by following, for example, theteaching of Lasko et al. (Lasko et al., Proc. Natl. Acad. Sci. USA89:6232-6236 (1992)). The regulatory sequences required for such acell-type specific activation will depend upon the particular cell typeof interest, and will be apparent to those of skill in the art. When itis desired that the polynucleotide encoding the fusion protein of theinvention be integrated into the chromosomal site of the endogenous genecorresponding to the Therapeutic protein portion or ablumin portion ofthe fusion protein of the invention, gene targeting is preferred.Briefly, when such a technique is to be utilized, vectors containingsome nucleotide sequences homologous to the endogenous gene are designedfor the purpose of integrating, via homologous recombination withchromosomal sequences, into and disrupting the function of thenucleotide sequence of the endogenous gene. The transgene may also beselectively introduced into a particular cell type, thus inactivatingthe endogenous gene in only that cell type, by following, for example,the teaching of Gu et al. (Gu et al., Science 265:103-106 (1994)). Theregulatory sequences required for such a cell-type specific inactivationwill depend upon the particular cell type of interest, and will beapparent to those of skill in the art.

Once transgenic animals have been generated, the expression of therecombinant gene may be assayed utilizing standard techniques. Initialscreening may be accomplished by Southern blot analysis or PCRtechniques to analyze animal tissues to verify that integration of thepolynucleotide encoding the fusion protein of the invention has takenplace. The level of mRNA expression of the polynucleotide encoding thefusion protein of the invention in the tissues of the transgenic animalsmay also be assessed using techniques which include, but are not limitedto, Northern blot analysis of tissue samples obtained from the animal,in situ hybridization analysis, and reverse transcriptase-PCR (rt-PCR).Samples of fusion protein-expressing tissue may also be evaluatedimmunocytochemically or immunohistochemically using antibodies specificfor the fusion protein.

Once the founder animals are produced, they may be bred, inbred,outbred, or crossbred to produce colonies of the particular animal.Examples of such breeding strategies include, but are not limited to:outbreeding of founder animals with more than one integration site inorder to establish separate lines; inbreeding of separate lines in orderto produce compound transgenics that express the transgene at higherlevels because of the effects of additive expression of each transgene;crossing of heterozygous transgenic animals to produce animalshomozygous for a given integration site in order to both augmentexpression and eliminate the need for screening of animals by DNAanalysis; crossing of separate homozygous lines to produce compoundheterozygous or homozygous lines; and breeding to place the transgene(i.e., polynucleotide encoding an albumin fusion protein of theinvention) on a distinct background that is appropriate for anexperimental model of interest.

Transgenic animals of the invention have uses which include, but are notlimited to, animal model systems useful in elaborating the biologicalfunction of fusion proteins of the invention and the Therapeutic proteinand/or albumin component of the fusion protein of the invention,studying conditions and/or disorders associated with aberrantexpression, and in screening for compounds effective in amelioratingsuch conditions and/or disorders.

Example 66 Assays Detecting Stimulation or Inhibition of B CellProliferation and Differentiation

Generation of functional humoral immune responses requires both solubleand cognate signaling between B-lineage cells and theirmicroenvironment. Signals may impart a positive stimulus that allows aB-lineage cell to continue its programmed development, or a negativestimulus that instructs the cell to arrest its current developmentalpathway. To date, numerous stimulatory and inhibitory signals have beenfound to influence B cell responsiveness including IL-2, IL-4, IL-5,IL-6, IL-7, IL10, IL-13, IL-14 and IL-15. Interestingly, these signalsare by themselves weak effectors but can, in combination with variousco-stimulatory proteins, induce activation, proliferation,differentiation, homing, tolerance and death among B cell populations.

One of the best studied classes of B-cell co-stimulatory proteins is theTNF-superfamily. Within this family CD40, CD27, and CD30 along withtheir respective ligands CD154, CD70, and CD153 have been found toregulate a variety of immune responses. Assays which allow for thedetection and/or observation of the proliferation and differentiation ofthese B-cell populations and their precursors are valuable tools indetermining the effects various proteins may have on these B-cellpopulations in terms of proliferation and differentiation. Listed beloware two assays designed to allow for the detection of thedifferentiation, proliferation, or inhibition of B-cell populations andtheir precursors.

In Vitro Assay—Albumin fusion proteins of the invention (includingfusion proteins containing fragments or variants of Therapeutic proteinsand/or albumin or fragments or variants of albumin) can be assessed forits ability to induce activation, proliferation, differentiation orinhibition and/or death in B-cell populations and their precursors. Theactivity of an albumin fusion protein of the invention on purified humantonsillar B cells, measured qualitatively over the dose range from 0.1to 10,000 ng/mL, is assessed in a standard B-lymphocyte co-stimulationassay in which purified tonsillar B cells are cultured in the presenceof either formalin-fixed Staphylococcus aureus Cowan I (SAC) orimmobilized anti-human IgM antibody as the priming agent. Second signalssuch as IL-2 and IL-15 synergize with SAC and IgM crosslinking to elicitB cell proliferation as measured by tritiated-thymidine incorporation.Novel synergizing agents can be readily identified using this assay. Theassay involves isolating human tonsillar B cells by magnetic bead (MACS)depletion of CD3-positive cells. The resulting cell population isgreater than 95% B cells as assessed by expression of CD45R(B220).

Various dilutions of each sample are placed into individual wells of a96-well plate to which are added 10⁵ B-cells suspended in culture medium(RPMI 1640 containing 10% FBS, 5×10⁻⁵M 2ME, 100U/ml penicillin, 10 ug/mlstreptomycin, and 10⁻⁵ dilution of SAC) in a total volume of 150 ul.Proliferation or inhibition is quantitated by a 20 h pulse (1 uCi/well)with 3H-thymidine (6.7 Ci/mM) beginning 72h post factor addition. Thepositive and negative controls are IL2 and medium respectively.

In vivo Assay—BALB/c mice are injected (i.p.) twice per day with bufferonly, or 2 mg/Kg of an albumin fusion protein of the invention(including fusion proteins containing fragments or variants ofTherapeutic proteins and/or albumin or fragments or variants ofalbumin). Mice receive this treatment for 4 consecutive days, at whichtime they are sacrificed and various tissues and serum collected foranalyses. Comparison of H&E sections from normal spleens and spleenstreated with the albumin fusion protein of the invention identify theresults of the activity of the fusion protein on spleen cells, such asthe diffusion of peri-arterial lymphatic sheaths, and/or significantincreases in the nucleated cellularity of the red pulp regions, whichmay indicate the activation of the differentiation and proliferation ofB-cell populations. Immunohistochemical studies using a B cell marker,anti-CD45R(B220), are used to determine whether any physiologicalchanges to splenic cells, such as splenic disorganization, are due toincreased B-cell representation within loosely defined B-cell zones thatinfiltrate established T-cell regions.

Flow cytometric analyses of the spleens from mice treated with thealbumin fusion protein is used to indicate whether the albumin fusionprotein specifically increases the proportion of ThB+, CD45R(B220)dull Bcells over that which is observed in control mice.

Likewise, a predicted consequence of increased mature B-cellrepresentation in vivo is a relative increase in serum Ig titers.Accordingly, serum IgM and IgA levels are compared between buffer andfusion protein treated mice.

Example 67 T Cell Proliferation Assay

A CD3-induced proliferation assay is performed on PBMCs and is measuredby the uptake of ³H-thymidine. The assay is performed as follows.Ninety-six well plates are coated with 100 μl/well of mAb to CD3 (HIT3a,Pharmingen) or isotype-matched control mAb (B33.1) overnight at 4degrees C. (1 μg/ml in 0.05M bicarbonate buffer, pH 9.5), then washedthree times with PBS. PBMC are isolated by F/H gradient centrifugationfrom human peripheral blood and added to quadruplicate wells(5×10⁴/well) of mAb coated plates in RPMI containing 10% FCS and P/S inthe presence of varying concentrations of an albumin fusion protein ofthe invention (including fusion proteins containing fragments orvariants of Therapeutic proteins and/or albumin or fragments or variantsof albumin) (total volume 200 ul). Relevant protein buffer and mediumalone are controls. After 48 hr. culture at 37 degrees C., plates arespun for 2 min. at 1000 rpm and 100 μl of supernatant is removed andstored −20 degrees C. for measurement of IL-2 (or other cytokines) ifeffect on proliferation is observed. Wells are supplemented with 100 ulof medium containing 0.5 uCi of ³H-thymidine and cultured at 37 degreesC. for 18-24 hr. Wells are harvested and incorporation of ³H-thymidineused as a measure of proliferation. Anti-CD3 alone is the positivecontrol for proliferation. IL-2 (100 U/ml) is also used as a controlwhich enhances proliferation. Control antibody which does not induceproliferation of T cells is used as the negative control for the effectsof fusion proteins of the invention.

Example 68 Effect of Fusion Proteins of the Invention on the Expressionof MHC Class II, Costimulatory and Adhesion Molecules and CellDifferentiation of Monocytes and Monocyte-Derived Human Dendritic Cells

Dendritic cells are generated by the expansion of proliferatingprecursors found in the peripheral blood: adherent PBMC or elutriatedmonocytic fractions are cultured for 7-10 days with GM-CSF (50 ng/ml)and IL-4 (20 ng/ml). These dendritic cells have the characteristicphenotype of immature cells (expression of CD1, CD80, CD86, CD40 and MEWclass II antigens). Treatment with activating factors, such as TNF-α,causes a rapid change in surface phenotype (increased expression of MEWclass I and II, costimulatory and adhesion molecules, downregulation ofFCγRII, upregulation of CD83). These changes correlate with increasedantigen-presenting capacity and with functional maturation of thedendritic cells.

FACS analysis of surface antigens is performed as follows. Cells aretreated 1-3 days with increasing concentrations of an albumin fusionprotein of the invention or LPS (positive control), washed with PBScontaining 1% BSA and 0.02 mM sodium azide, and then incubated with 1:20dilution of appropriate FITC- or PE-labeled monoclonal antibodies for 30minutes at 4 degrees C. After an additional wash, the labeled cells areanalyzed by flow cytometry on a FACScan (Becton Dickinson).

Effect on the Production of Cytokines.

Cytokines generated by dendritic cells, in particular IL-12, areimportant in the initiation of T-cell dependent immune responses. IL-12strongly influences the development of Th1 helper T-cell immuneresponse, and induces cytotoxic T and NK cell function. An ELISA is usedto measure the IL-12 release as follows. Dendritic cells (10⁶/ml) aretreated with increasing concentrations of an albumin fusion protein ofthe invention for 24 hours. LPS (100 ng/ml) is added to the cell cultureas positive control. Supernatants from the cell cultures are thencollected and analyzed for IL-12 content using commercial ELISA kit(e.g., R & D Systems (Minneapolis, Minn.)). The standard protocolsprovided with the kits are used.

Effect on the Expression of MHC Class II, Costimulatory and AdhesionMolecules.

Three major families of cell surface antigens can be identified onmonocytes: adhesion molecules, molecules involved in antigenpresentation, and Fc receptor. Modulation of the expression of MHC classII antigens and other costimulatory molecules, such as B7 and ICAM-1,may result in changes in the antigen presenting capacity of monocytesand ability to induce T cell activation. Increased expression of Fcreceptors may correlate with improved monocyte cytotoxic activity,cytokine release and phagocytosis.

FACS analysis is used to examine the surface antigens as follows.Monocytes are treated 1-5 days with increasing concentrations of analbumin fusion protein of the invention or LPS (positive control),washed with PBS containing 1% BSA and 0.02 mM sodium azide, and thenincubated with 1:20 dilution of appropriate FITC- or PE-labeledmonoclonal antibodies for 30 minutes at 4 degrees C. After an additionalwash, the labeled cells are analyzed by flow cytometry on a FACScan(Becton Dickinson).

Monocyte Activation and/or Increased Survival.

Assays for molecules that activate (or alternatively, inactivate)monocytes and/or increase monocyte survival (or alternatively, decreasemonocyte survival) are known in the art and may routinely be applied todetermine whether a molecule of the invention functions as an inhibitoror activator of monocytes. Albumin fusion proteins of the invention canbe screened using the three assays described below. For each of theseassays, Peripheral blood mononuclear cells (PBMC) are purified fromsingle donor leukopacks (American Red Cross, Baltimore, Md.) bycentrifugation through a Histopaque gradient (Sigma). Monocytes areisolated from PBMC by counterflow centrifugal elutriation.

Monocyte Survival Assay.

Human peripheral blood monocytes progressively lose viability whencultured in absence of serum or other stimuli. Their death results frominternally regulated processes (apoptosis). Addition to the culture ofactivating factors, such as TNF-alpha dramatically improves cellsurvival and prevents DNA fragmentation. Propidium iodide (PI) stainingis used to measure apoptosis as follows. Monocytes are cultured for 48hours in polypropylene tubes in serum-free medium (positive control), inthe presence of 100 ng/ml TNF-alpha (negative control), and in thepresence of varying concentrations of the fusion protein to be tested.Cells are suspended at a concentration of 2×10⁶/ml in PBS containing PIat a final concentration of 5 μg/ml, and then incubated at roomtemperature for 5 minutes before FACScan analysis. PI uptake has beendemonstrated to correlate with DNA fragmentation in this experimentalparadigm.

Effect on Cytokine Release.

An important function of monocytes/macrophages is their regulatoryactivity on other cellular populations of the immune system through therelease of cytokines after stimulation. An ELISA to measure cytokinerelease is performed as follows. Human monocytes are incubated at adensity of 5×10⁵ cells/ml with increasing concentrations of an albuminfusion protein of the invention and under the same conditions, but inthe absence of the fusion protein. For IL-12 production, the cells areprimed overnight with IFN (100 U/ml) in the presence of the fusionprotein. LPS (10 ng/ml) is then added. Conditioned media are collectedafter 24 h and kept frozen until use. Measurement of TNF-alpha, IL-10,MCP-1 and IL-8 is then performed using a commercially available ELISAkit (e.g., R & D Systems (Minneapolis, Minn.)) and applying the standardprotocols provided with the kit.

Oxidative Burst.

Purified monocytes are plated in 96-w plate at 2-1×10⁵ cell/well.Increasing concentrations of an albumin fusion protein of the inventionare added to the wells in a total volume of 0.2 ml culture medium (RPMI1640+10% FCS, glutamine and antibiotics). After 3 days incubation, theplates are centrifuged and the medium is removed from the wells. To themacrophage monolayers, 0.2 ml per well of phenol red solution (140 mMNaCl, 10 mM potassium phosphate buffer pH 7.0, 5.5 mM dextrose, 0.56 mMphenol red and 19 U/ml of HRPO) is added, together with the stimulant(200 nM PMA). The plates are incubated at 37° C. for 2 hours and thereaction is stopped by adding 20 μl 1N NaOH per well. The absorbance isread at 610 nm. To calculate the amount of H₂O₂ produced by themacrophages, a standard curve of a H₂O₂ solution of known molarity isperformed for each experiment.

Example 69 Biological Effects of Fusion Proteins of the InventionAstrocyte and Neuronal Assays.

Albumin fusion proteins of the invention can be tested for activity inpromoting the survival, neurite outgrowth, or phenotypic differentiationof cortical neuronal cells and for inducing the proliferation of glialfibrillary acidic protein immunopositive cells, astrocytes. Theselection of cortical cells for the bioassay is based on the prevalentexpression of FGF-1 and FGF-2 in cortical structures and on thepreviously reported enhancement of cortical neuronal survival resultingfrom FGF-2 treatment. A thymidine incorporation assay, for example, canbe used to elucidate an albumin fusion protein of the invention'sactivity on these cells.

Moreover, previous reports describing the biological effects of FGF-2(basic FGF) on cortical or hippocampal neurons in vitro havedemonstrated increases in both neuron survival and neurite outgrowth(Walicke et al., “Fibroblast growth factor promotes survival ofdissociated hippocampal neurons and enhances neurite extension.” Proc.Natl. Acad. Sci. USA 83:3012-3016. (1986), assay herein incorporated byreference in its entirety). However, reports from experiments done onPC-12 cells suggest that these two responses are not necessarilysynonymous and may depend on not only which FGF is being tested but alsoon which receptor(s) are expressed on the target cells. Using theprimary cortical neuronal culture paradigm, the ability of an albuminfusion protein of the invention to induce neurite outgrowth can becompared to the response achieved with FGF-2 using, for example, athymidine incorporation assay.

Fibroblast and Endothelial Cell Assays.

Human lung fibroblasts are obtained from Clonetics (San Diego, Calif.)and maintained in growth media from Clonetics. Dermal microvascularendothelial cells are obtained from Cell Applications (San Diego,Calif.). For proliferation assays, the human lung fibroblasts and dermalmicrovascular endothelial cells can be cultured at 5,000 cells/well in a96-well plate for one day in growth medium. The cells are then incubatedfor one day in 0.1% BSA basal medium. After replacing the medium withfresh 0.1% BSA medium, the cells are incubated with the test fusionprotein of the invention proteins for 3 days. Alamar Blue (AlamarBiosciences, Sacramento, Calif.) is added to each well to a finalconcentration of 10%. The cells are incubated for 4 hr. Cell viabilityis measured by reading in a CytoFluor fluorescence reader. For the PGE₂assays, the human lung fibroblasts are cultured at 5,000 cells/well in a96-well plate for one day. After a medium change to 0.1% BSA basalmedium, the cells are incubated with FGF-2 or fusion protein of theinvention with or without IL-1α for 24 hours. The supernatants arecollected and assayed for PGE₂ by EIA kit (Cayman, Ann Arbor, Mich.).For the IL-6 assays, the human lung fibroblasts are cultured at 5,000cells/well in a 96-well plate for one day. After a medium change to 0.1%BSA basal medium, the cells are incubated with FGF-2 or with or withoutan albumin fusion protein of the invention and/or IL-1α for 24 hours.The supernatants are collected and assayed for IL-6 by ELISA kit(Endogen, Cambridge, Mass.).

Human lung fibroblasts are cultured with FGF-2 or an albumin fusionprotein of the invention for 3 days in basal medium before the additionof Alamar Blue to assess effects on growth of the fibroblasts. FGF-2should show a stimulation at 10-2500 ng/ml which can be used to comparestimulation with the fusion protein of the invention.

Cell Proliferation Based on [3H]Thymidine Incorporation

The following [3H]Thymidine incorporation assay can be used to measurethe effect of a Therapeutic proteins, e.g., growth factor proteins, onthe proliferation of cells such as fibroblast cells, epithelial cells orimmature muscle cells.

Sub-confluent cultures are arrested in G1 phase by an 18 h incubation inserum-free medium. Therapeutic proteins are then added for 24 h andduring the last 4 h, the cultures are labeled with [3H]thymidine, at afinal concentration of 0.33 μM (25 Ci/mmol, Amersham, Arlington Heights,Ill.). The incorporated [3H]thymidine is precipitated with ice-cold 10%trichloroacetic acid for 24 h. Subsequently, the cells are rinsedsequentially with ice-cold 10% trichloroacetic acid and then withice-cold water. Following lysis in 0.5 M NaOH, the lysates and PBSrinses (500 ml) are pooled, and the amount of radioactivity is measured.

Parkinson Models.

The loss of motor function in Parkinson's disease is attributed to adeficiency of striatal dopamine resulting from the degeneration of thenigrostriatal dopaminergic projection neurons. An animal model forParkinson's that has been extensively characterized involves thesystemic administration of 1-methyl-4 phenyl 1,2,3,6-tetrahydropyridine(MPTP). In the CNS, MPTP is taken-up by astrocytes and catabolized bymonoamine oxidase B to 1-methyl-4-phenyl pyridine (MPP⁺) and released.Subsequently, MPP⁺ is actively accumulated in dopaminergic neurons bythe high-affinity reuptake transporter for dopamine. MPP⁺ is thenconcentrated in mitochondria by the electrochemical gradient andselectively inhibits nicotidamide adenine disphosphate: ubiquinoneoxidoreductionase (complex I), thereby interfering with electrontransport and eventually generating oxygen radicals.

It has been demonstrated in tissue culture paradigms that FGF-2 (basicFGF) has trophic activity towards nigral dopaminergic neurons (Ferrariet al., Dev. Biol. 1989). Recently, Dr. Unsicker's group hasdemonstrated that administering FGF-2 in gel foam implants in thestriatum results in the near complete protection of nigral dopaminergicneurons from the toxicity associated with MPTP exposure (Otto andUnsicker, J. Neuroscience, 1990).

Based on the data with FGF-2, an albumin fusion protein of the inventioncan be evaluated to determine whether it has an action similar to thatof FGF-2 in enhancing dopaminergic neuronal survival in vitro and it canalso be tested in vivo for protection of dopaminergic neurons in thestriatum from the damage associated with MPTP treatment. The potentialeffect of an albumin fusion protein of the invention is first examinedin vitro in a dopaminergic neuronal cell culture paradigm. The culturesare prepared by dissecting the midbrain floor plate from gestation day14 Wistar rat embryos. The tissue is dissociated with trypsin and seededat a density of 200,000 cells/cm² on polyorthinine-laminin coated glasscoverslips. The cells are maintained in Dulbecco's Modified Eagle'smedium and F12 medium containing hormonal supplements (N1). The culturesare fixed with paraformaldehyde after 8 days in vitro and are processedfor tyrosine hydroxylase, a specific marker for dopaminergic neurons,immunohistochemical staining. Dissociated cell cultures are preparedfrom embryonic rats. The culture medium is changed every third day andthe factors are also added at that time.

Since the dopaminergic neurons are isolated from animals at gestationday 14, a developmental time which is past the stage when thedopaminergic precursor cells are proliferating, an increase in thenumber of tyrosine hydroxylase immunopositive neurons would represent anincrease in the number of dopaminergic neurons surviving in vitro.Therefore, if a therapeutic protein of the invention acts to prolong thesurvival of dopaminergic neurons, it would suggest that the fusionprotein may be involved in Parkinson's Disease.

Example 70 The Effect of Albumin Fusion Proteins of the Invention on theGrowth of Vascular Endothelial Cells

On day 1, human umbilical vein endothelial cells (HUVEC) are seeded at2-5×10⁴ cells/35 mm dish density in M199 medium containing 4% fetalbovine serum (FBS), 16 units/ml heparin, and 50 units/ml endothelialcell growth supplements (ECGS, Biotechnique, Inc.). On day 2, the mediumis replaced with M199 containing 10% FBS, 8 units/ml heparin. An albuminfusion protein of the invention, and positive controls, such as VEGF andbasic FGF (bFGF) are added, at varying concentrations. On days 4 and 6,the medium is replaced. On day 8, cell number is determined with aCoulter Counter.

An increase in the number of HUVEC cells indicates that the fusionprotein may proliferate vascular endothelial cells, while a decrease inthe number of HUVEC cells indicates that the fusion protein inhibitsvascular endothelial cells.

Example 71 Rat Corneal Wound Healing Model

This animal model shows the effect of an albumin fusion protein of theinvention on neovascularization. The experimental protocol includes:

Making a 1-1.5 mm long incision from the center of cornea into thestromal layer.

Inserting a spatula below the lip of the incision facing the outercorner of the eye.

Making a pocket (its base is 1-1.5 mm form the edge of the eye).

Positioning a pellet, containing 50 ng-5 ug of an albumin fusion proteinof the invention, within the pocket.

Treatment with an albumin fusion protein of the invention can also beapplied topically to the corneal wounds in a dosage range of 20 mg-500mg (daily treatment for five days).

Example 72 Diabetic Mouse and Glucocorticoid-Impaired Wound HealingModels Diabetic db+/db+ Mouse Model

To demonstrate that an albumin fusion protein of the inventionaccelerates the healing process, the genetically diabetic mouse model ofwound healing is used. The full thickness wound healing model in thedb+/db+ mouse is a well characterized, clinically relevant andreproducible model of impaired wound healing. Healing of the diabeticwound is dependent on formation of granulation tissue andre-epithelialization rather than contraction (Gartner, M. H. et al., J.Surg. Res. 52:389 (1992); Greenhalgh, D. G. et al., Am. J. Pathol.136:1235 (1990)).

The diabetic animals have many of the characteristic features observedin Type II diabetes mellitus. Homozygous (db+/db+) mice are obese incomparison to their normal heterozygous (db+/+m) littermates. Mutantdiabetic (db+/db+) mice have a single autosomal recessive mutation onchromosome 4 (db+) (Coleman et al. Proc. Natl. Acad. Sci. USA 77:283-293(1982)). Animals show polyphagia, polydipsia and polyuria. Mutantdiabetic mice (db+/db+) have elevated blood glucose, increased or normalinsulin levels, and suppressed cell-mediated immunity (Mandel et al., J.Immunol. 120:1375 (1978); Debray-Sachs, M. et al., Clin. Exp. Immunol.51(1):1-7 (1983); Leiter et al., Am. J. of Pathol. 114:46-55 (1985)).Peripheral neuropathy, myocardial complications, and microvascularlesions, basement membrane thickening and glomerular filtrationabnormalities have been described in these animals (Norido, F. et al.,Exp. Neurol. 83(2):221-232 (1984); Robertson et al., Diabetes29(1):60-67 (1980); Giacomelli et al., Lab Invest. 40(4):460-473 (1979);Coleman, D. L., Diabetes 31 (Suppl):1-6 (1982)). These homozygousdiabetic mice develop hyperglycemia that is resistant to insulinanalogous to human type II diabetes (Mandel et al., J. Immunol.120:1375-1377 (1978)).

The characteristics observed in these animals suggests that healing inthis model may be similar to the healing observed in human diabetes(Greenhalgh, et al., Am. J. of Pathol. 136:1235-1246 (1990)).

Genetically diabetic female C57BL/KsJ (db+/db+) mice and theirnon-diabetic (db+/+m) heterozygous littermates are used in this study(Jackson Laboratories). The animals are purchased at 6 weeks of age andare 8 weeks old at the beginning of the study. Animals are individuallyhoused and received food and water ad libitum. All manipulations areperformed using aseptic techniques. The experiments are conductedaccording to the rules and guidelines of Human Genome Sciences, Inc.Institutional Animal Care and Use Committee and the Guidelines for theCare and Use of Laboratory Animals.

Wounding protocol is performed according to previously reported methods(Tsuboi, R. and Rifkin, D. B., J. Exp. Med. 172:245-251 (1990)).Briefly, on the day of wounding, animals are anesthetized with anintraperitoneal injection of Avertin (0.01 mg/mL), 2,2,2-tribromoethanoland 2-methyl-2-butanol dissolved in deionized water. The dorsal regionof the animal is shaved and the skin washed with 70% ethanol solutionand iodine. The surgical area is dried with sterile gauze prior towounding. An 8 mm full-thickness wound is then created using a Keyestissue punch. Immediately following wounding, the surrounding skin isgently stretched to eliminate wound expansion. The wounds are left openfor the duration of the experiment. Application of the treatment isgiven topically for 5 consecutive days commencing on the day ofwounding. Prior to treatment, wounds are gently cleansed with sterilesaline and gauze sponges.

Wounds are visually examined and photographed at a fixed distance at theday of surgery and at two day intervals thereafter. Wound closure isdetermined by daily measurement on days 1-5 and on day 8. Wounds aremeasured horizontally and vertically using a calibrated Jameson caliper.Wounds are considered healed if granulation tissue is no longer visibleand the wound is covered by a continuous epithelium.

An albumin fusion protein of the invention is administered using at arange different doses, from 4 mg to 500 mg per wound per day for 8 daysin vehicle. Vehicle control groups received 50 mL of vehicle solution.

Animals are euthanized on day 8 with an intraperitoneal injection ofsodium pentobarbital (300 mg/kg). The wounds and surrounding skin arethen harvested for histology and immunohistochemistry. Tissue specimensare placed in 10% neutral buffered formalin in tissue cassettes betweenbiopsy sponges for further processing.

Three groups of 10 animals each (5 diabetic and 5 non-diabetic controls)are evaluated: 1) Vehicle placebo control, 2) untreated group, and 3)treated group.

Wound closure is analyzed by measuring the area in the vertical andhorizontal axis and obtaining the total square area of the wound.Contraction is then estimated by establishing the differences betweenthe initial wound area (day 0) and that of post treatment (day 8). Thewound area on day 1 is 64 mm², the corresponding size of the dermalpunch. Calculations are made using the following formula:

[Open area on day 8]−[Open area on day 1]/[Open area on day 1]  a.

Specimens are fixed in 10% buffered formalin and paraffin embeddedblocks are sectioned perpendicular to the wound surface (5 mm) and cutusing a Reichert-Jung microtome. Routine hematoxylin-eosin (H&E)staining is performed on cross-sections of bisected wounds. Histologicexamination of the wounds are used to assess whether the healing processand the morphologic appearance of the repaired skin is altered bytreatment with an albumin fusion protein of the invention. Thisassessment included verification of the presence of cell accumulation,inflammatory cells, capillaries, fibroblasts, re-epithelialization andepidermal maturity (Greenhalgh, D. G. et al., Am. J. Pathol. 136:1235(1990)). A calibrated lens micrometer is used by a blinded observer.

Tissue sections are also stained immunohistochemically with a polyclonalrabbit anti-human keratin antibody using ABC Elite detection system.Human skin is used as a positive tissue control while non-immune IgG isused as a negative control. Keratinocyte growth is determined byevaluating the extent of reepithelialization of the wound using acalibrated lens micrometer.

Proliferating cell nuclear antigen/cyclin (PCNA) in skin specimens isdemonstrated by using anti-PCNA antibody (1:50) with an ABC Elitedetection system. Human colon cancer served as a positive tissue controland human brain tissue is used as a negative tissue control. Eachspecimen included a section with omission of the primary antibody andsubstitution with non-immune mouse IgG. Ranking of these sections isbased on the extent of proliferation on a scale of 0-8, the lower sideof the scale reflecting slight proliferation to the higher sidereflecting intense proliferation.

Experimental data are analyzed using an unpaired t test. A p value of<0.05 is considered significant.

Steroid Impaired Rat Model

The inhibition of wound healing by steroids has been well documented invarious in vitro and in vivo systems (Wahl, Glucocorticoids and Woundhealing. In: Anti-Inflammatory Steroid Action: Basic and ClinicalAspects. 280-302 (1989); Wahl et al., J. Immunol. 115: 476-481 (1975);Werb et al., J. Exp. Med. 147:1684-1694 (1978)). Glucocorticoids retardwound healing by inhibiting angiogenesis, decreasing vascularpermeability (Ebert et al., An. Intern. Med. 37:701-705 (1952)),fibroblast proliferation, and collagen synthesis (Beck et al., GrowthFactors. 5: 295-304 (1991); Haynes et al., J. Clin. Invest. 61: 703-797(1978)) and producing a transient reduction of circulating monocytes(Haynes et al., J. Clin. Invest. 61: 703-797 (1978); Wahl,“Glucocorticoids and wound healing”, In: Antiinflammatory SteroidAction: Basic and Clinical Aspects, Academic Press, New York, pp.280-302 (1989)). The systemic administration of steroids to impairedwound healing is a well establish phenomenon in rats (Beck et al.,Growth Factors. 5: 295-304 (1991); Haynes et al., J. Clin. Invest. 61:703-797 (1978); Wahl, “Glucocorticoids and wound healing”, In:Antiinflammatory Steroid Action: Basic and Clinical Aspects, AcademicPress, New York, pp. 280-302 (1989); Pierce et al., Proc. Natl. Acad.Sci. USA 86: 2229-2233 (1989)).

To demonstrate that an albumin fusion protein of the invention canaccelerate the healing process, the effects of multiple topicalapplications of the fusion protein on full thickness excisional skinwounds in rats in which healing has been impaired by the systemicadministration of methylprednisolone is assessed.

Young adult male Sprague Dawley rats weighing 250-300 g (Charles RiverLaboratories) are used in this example. The animals are purchased at 8weeks of age and are 9 weeks old at the beginning of the study. Thehealing response of rats is impaired by the systemic administration ofmethylprednisolone (17 mg/kg/rat intramuscularly) at the time ofwounding. Animals are individually housed and received food and water adlibitum. All manipulations are performed using aseptic techniques. Thisstudy is conducted according to the rules and guidelines of Human GenomeSciences, Inc. Institutional Animal Care and Use Committee and theGuidelines for the Care and Use of Laboratory Animals.

The wounding protocol is followed according to that described above. Onthe day of wounding, animals are anesthetized with an intramuscularinjection of ketamine (50 mg/kg) and xylazine (5 mg/kg). The dorsalregion of the animal is shaved and the skin washed with 70% ethanol andiodine solutions. The surgical area is dried with sterile gauze prior towounding. An 8 mm full-thickness wound is created using a Keyes tissuepunch. The wounds are left open for the duration of the experiment.Applications of the testing materials are given topically once a day for7 consecutive days commencing on the day of wounding and subsequent tomethylprednisolone administration. Prior to treatment, wounds are gentlycleansed with sterile saline and gauze sponges.

Wounds are visually examined and photographed at a fixed distance at theday of wounding and at the end of treatment. Wound closure is determinedby daily measurement on days 1-5 and on day 8. Wounds are measuredhorizontally and vertically using a calibrated Jameson caliper. Woundsare considered healed if granulation tissue is no longer visible and thewound is covered by a continuous epithelium.

The fusion protein of the invention is administered using at a rangedifferent doses, from 4 mg to 500 mg per wound per day for 8 days invehicle. Vehicle control groups received 50 mL of vehicle solution.

Animals are euthanized on day 8 with an intraperitoneal injection ofsodium pentobarbital (300 mg/kg). The wounds and surrounding skin arethen harvested for histology. Tissue specimens are placed in 10% neutralbuffered formalin in tissue cassettes between biopsy sponges for furtherprocessing.

Three groups of 10 animals each (5 with methylprednisolone and 5 withoutglucocorticoid) are evaluated: 1) Untreated group 2) Vehicle placebocontrol 3) treated groups.

Wound closure is analyzed by measuring the area in the vertical andhorizontal axis and obtaining the total area of the wound. Closure isthen estimated by establishing the differences between the initial woundarea (day 0) and that of post treatment (day 8). The wound area on day 1is 64 mm², the corresponding size of the dermal punch. Calculations aremade using the following formula:

[Open area on day 8]−[Open area on day 1]/[Open area on day 1]  a.

Specimens are fixed in 10% buffered formalin and paraffin embeddedblocks are sectioned perpendicular to the wound surface (5 mm) and cutusing an Olympus microtome. Routine hematoxylin-eosin (H&E) staining isperformed on cross-sections of bisected wounds. Histologic examinationof the wounds allows assessment of whether the healing process and themorphologic appearance of the repaired skin is improved by treatmentwith an albumin fusion protein of the invention. A calibrated lensmicrometer is used by a blinded observer to determine the distance ofthe wound gap.

Experimental data are analyzed using an unpaired t test. A p value of<0.05 is considered significant.

Example 73 Lymphedema Animal Model

The purpose of this experimental approach is to create an appropriateand consistent lymphedema model for testing the therapeutic effects ofan albumin fusion protein of the invention in lymphangiogenesis andre-establishment of the lymphatic circulatory system in the rat hindlimb. Effectiveness is measured by swelling volume of the affected limb,quantification of the amount of lymphatic vasculature, total bloodplasma protein, and histopathology. Acute lymphedema is observed for7-10 days. Perhaps more importantly, the chronic progress of the edemais followed for up to 3-4 weeks.

Prior to beginning surgery, blood sample is drawn for proteinconcentration analysis. Male rats weighing approximately −350 g aredosed with Pentobarbital. Subsequently, the right legs are shaved fromknee to hip. The shaved area is swabbed with gauze soaked in 70% EtOH.Blood is drawn for serum total protein testing. Circumference andvolumetric measurements are made prior to injecting dye into paws aftermarking 2 measurement levels (0.5 cm above heel, at mid-pt of dorsalpaw). The intradermal dorsum of both right and left paws are injectedwith 0.05 ml of 1% Evan's Blue. Circumference and volumetricmeasurements are then made following injection of dye into paws.

Using the knee joint as a landmark, a mid-leg inguinal incision is madecircumferentially allowing the femoral vessels to be located. Forcepsand hemostats are used to dissect and separate the skin flaps. Afterlocating the femoral vessels, the lymphatic vessel that runs along sideand underneath the vessel(s) is located. The main lymphatic vessels inthis area are then electrically coagulated or suture ligated.

Using a microscope, muscles in back of the leg (near the semitendinosisand adductors) are bluntly dissected. The popliteal lymph node is thenlocated. The 2 proximal and 2 distal lymphatic vessels and distal bloodsupply of the popliteal node are then ligated by suturing. The popliteallymph node, and any accompanying adipose tissue, is then removed bycutting connective tissues.

Care is taken to control any mild bleeding resulting from thisprocedure. After lymphatics are occluded, the skin flaps are sealed byusing liquid skin (Vetbond) (AJ Buck). The separated skin edges aresealed to the underlying muscle tissue while leaving a gap of ˜0.5 cmaround the leg. Skin also may be anchored by suturing to underlyingmuscle when necessary.

To avoid infection, animals are housed individually with mesh (nobedding). Recovering animals are checked daily through the optimaledematous peak, which typically occurred by day 5-7. The plateauedematous peak are then observed. To evaluate the intensity of thelymphedema, the circumference and volumes of 2 designated places on eachpaw before operation and daily for 7 days are measured. The effect ofplasma proteins on lymphedema is determined and whether protein analysisis a useful testing perimeter is also investigated. The weights of bothcontrol and edematous limbs are evaluated at 2 places. Analysis isperformed in a blind manner.

Circumference Measurements: Under brief gas anesthetic to prevent limbmovement, a cloth tape is used to measure limb circumference.Measurements are done at the ankle bone and dorsal paw by 2 differentpeople and those 2 readings are averaged. Readings are taken from bothcontrol and edematous limbs.

Volumetric Measurements: On the day of surgery, animals are anesthetizedwith Pentobarbital and are tested prior to surgery. For dailyvolumetrics animals are under brief halothane anesthetic (rapidimmobilization and quick recovery), and both legs are shaved and equallymarked using waterproof marker on legs. Legs are first dipped in water,then dipped into instrument to each marked level then measured by Buxcoedema software (Chen/Victor). Data is recorded by one person, while theother is dipping the limb to marked area.

Blood-plasma protein measurements: Blood is drawn, spun, and serumseparated prior to surgery and then at conclusion for total protein andCa2⁺ comparison.

Limb Weight Comparison: After drawing blood, the animal is prepared fortissue collection. The limbs are amputated using a quillitine, then bothexperimental and control legs are cut at the ligature and weighed. Asecond weighing is done as the tibio-cacaneal joint is disarticulatedand the foot is weighed.

Histological Preparations: The transverse muscle located behind the knee(popliteal) area is dissected and arranged in a metal mold, filled withfreezeGel, dipped into cold methylbutane, placed into labeled samplebags at −80EC until sectioning. Upon sectioning, the muscle is observedunder fluorescent microscopy for lymphatics.

Example 74 Suppression of TNF Alpha-Induced Adhesion Molecule Expressionby an Albumin Fusion Protein of the Invention

The recruitment of lymphocytes to areas of inflammation and angiogenesisinvolves specific receptor-ligand interactions between cell surfaceadhesion molecules (CAMs) on lymphocytes and the vascular endothelium.The adhesion process, in both normal and pathological settings, followsa multi-step cascade that involves intercellular adhesion molecule-1(ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and endothelialleukocyte adhesion molecule-1 (E-selectin) expression on endothelialcells (EC). The expression of these molecules and others on the vascularendothelium determines the efficiency with which leukocytes may adhereto the local vasculature and extravasate into the local tissue duringthe development of an inflammatory response. The local concentration ofcytokines and growth factor participate in the modulation of theexpression of these CAMs.

Tumor necrosis factor alpha (TNF-a), a potent proinflammatory cytokine,is a stimulator of all three CAMs on endothelial cells and may beinvolved in a wide variety of inflammatory responses, often resulting ina pathological outcome.

The potential of an albumin fusion protein of the invention to mediate asuppression of TNF-a induced CAM expression can be examined. A modifiedELISA assay which uses ECs as a solid phase absorbent is employed tomeasure the amount of CAM expression on TNF-a treated ECs whenco-stimulated with a member of the FGF family of proteins.

To perform the experiment, human umbilical vein endothelial cell (HUVEC)cultures are obtained from pooled cord harvests and maintained in growthmedium (EGM-2; Clonetics, San Diego, Calif.) supplemented with 10% FCSand 1% penicillin/streptomycin in a 37 degree C. humidified incubatorcontaining 5% CO₂. HUVECs are seeded in 96-well plates at concentrationsof 1×10⁴ cells/well in EGM medium at 37 degree C. for 18-24 hrs or untilconfluent. The monolayers are subsequently washed 3 times with aserum-free solution of RPMI-1640 supplemented with 100 U/ml penicillinand 100 mg/ml streptomycin, and treated with a given cytokine and/orgrowth factor(s) for 24 h at 37 degree C. Following incubation, thecells are then evaluated for CAM expression.

Human Umbilical Vein Endothelial cells (HUVECs) are grown in a standard96 well plate to confluence. Growth medium is removed from the cells andreplaced with 90 ul of 199 Medium (10% FBS). Samples for testing andpositive or negative controls are added to the plate in triplicate (in10 ul volumes). Plates are incubated at 37 degree C. for either 5 h(selectin and integrin expression) or 24 h (integrin expression only).Plates are aspirated to remove medium and 100 μl of 0.1%paraformaldehyde-PBS (with Ca⁺⁺ and Mg⁺⁺) is added to each well. Platesare held at 4° C. for 30 min.

Fixative is then removed from the wells and wells are washed 1× withPBS(+Ca,Mg)+0.5% BSA and drained. Do not allow the wells to dry. Add 10μl of diluted primary antibody to the test and control wells.Anti-ICAM-1-Biotin, Anti-VCAM-1-Biotin and Anti-E-selectin-Biotin areused at a concentration of 10 μg/ml (1:10 dilution of 0.1 mg/ml stockantibody). Cells are incubated at 37° C. for 30 min. in a humidifiedenvironment. Wells are washed ×3 with PBS(+Ca,Mg)+0.5% BSA.

Then add 20 μl of diluted ExtrAvidin-Alkaline Phosphotase (1:5,000dilution) to each well and incubated at 37° C. for 30 min. Wells arewashed ×3 with PBS(+Ca,Mg)+0.5% BSA. 1 tablet of p-Nitrophenol PhosphatepNPP is dissolved in 5 ml of glycine buffer (pH 10.4). 100 μl of pNPPsubstrate in glycine buffer is added to each test well. Standard wellsin triplicate are prepared from the working dilution of theExtrAvidin-Alkaline Phosphotase in glycine buffer: 1:5,000) (10⁰) >10^(−0.5)>10⁻¹>10^(−1.5). 5 μl of each dilution is added to triplicatewells and the resulting AP content in each well is 5.50 ng, 1.74 ng,0.55 ng, 0.18 ng. 100 μl of pNNP reagent must then be added to each ofthe standard wells. The plate must be incubated at 37° C. for 4 h. Avolume of 50 μl of 3M NaOH is added to all wells. The results arequantified on a plate reader at 405 nm. The background subtractionoption is used on blank wells filled with glycine buffer only. Thetemplate is set up to indicate the concentration of AP-conjugate in eachstandard well [5.50 ng; 1.74 ng; 0.55 ng; 0.18 ng]. Results areindicated as amount of bound AP-conjugate in each sample.

Example 75 Construction of GAS Reporter Construct

One signal transduction pathway involved in the differentiation andproliferation of cells is called the Jaks-STATs pathway. Activatedproteins in the Jaks-STATs pathway bind to gamma activation site “GAS”elements or interferon-sensitive responsive element (“ISRE”), located inthe promoter of many genes. The binding of a protein to these elementsalter the expression of the associated gene.

GAS and ISRE elements are recognized by a class of transcription factorscalled Signal Transducers and Activators of Transcription, or “STATs.”There are six members of the STATs family. Stat1 and Stat3 are presentin many cell types, as is Stat2 (as response to IFN-alpha iswidespread). Stat4 is more restricted and is not in many cell typesthough it has been found in T helper class I, cells after treatment withIL-12. Stat5 was originally called mammary growth factor, but has beenfound at higher concentrations in other cells including myeloid cells.It can be activated in tissue culture cells by many cytokines.

The STATs are activated to translocate from the cytoplasm to the nucleusupon tyrosine phosphorylation by a set of kinases known as the JanusKinase (“Jaks”) family. Jaks represent a distinct family of solubletyrosine kinases and include Tyk2, Jak1, Jak2, and Jak3. These kinasesdisplay significant sequence similarity and are generally catalyticallyinactive in resting cells.

The Jaks are activated by a wide range of receptors summarized in theTable below. (Adapted from review by Schidler and Darnell, Ann. Rev.Biochem. 64:621-51 (1995)). A cytokine receptor family, capable ofactivating Jaks, is divided into two groups: (a) Class 1 includesreceptors for IL-2, IL-3, IL-4, IL-6, IL-7, IL-9, IL-11, IL-12, IL-15,Epo, PRL, GH, G-CSF, GM-CSF, LIF, CNTF, and thrombopoietin; and (b)Class 2 includes IFN-a, IFN-g, and IL-10. The Class 1 receptors share aconserved cysteine motif (a set of four conserved cysteines and onetryptophan) and a WSXWS motif (a membrane proximal region encodingTrp-Ser-Xaa-Trp-Ser (SEQ ID NO: 1113)).

Thus, on binding of a ligand to a receptor, Jaks are activated, which inturn activate STATs, which then translocate and bind to GAS elements.This entire process is encompassed in the Jaks-STATs signal transductionpathway. Therefore, activation of the Jaks-STATs pathway, reflected bythe binding of the GAS or the ISRE element, can be used to indicateproteins involved in the proliferation and differentiation of cells. Forexample, growth factors and cytokines are known to activate theJaks-STATs pathway (See Table 5, below). Thus, by using GAS elementslinked to reporter molecules, activators of the Jaks-STATs pathway canbe identified.

TABLE 5 JAKs Ligand tyk2 Jak1 Jak2 Jak3 STATS GAS(elements) or ISRE IFNfamily IFN-a/B + + − − 1, 2, 3 ISRE IFN-g + + − 1 GAS (IRF1 > Lys6 >IFP) Il-10 + ? ? − 1, 3 gp130 family IL-6 (Pleiotropic) + + + ? 1, 3GAS(IRF1 > Lys6 > IFP) Il-11(Pleiotropic) ? + ? ? 1, 3 OnM(Pleiotropic)? + + ? 1, 3 LIF(Pleiotropic) ? + + ? 1, 3 CNTF(Pleiotropic) −/+ + + ?1, 3 G-CSF(Pleiotropic) ? + ? ? 1, 3 IL-12(Pleiotropic) + − + + 1, 3 g-Cfamily IL-2 (lymphocytes) − + − + 1, 3, 5 GAS IL-4 (lymph/myeloid) − +− + 6 GAS(IRF1 = IFP >> Ly6)(IgH) IL-7 (lymphocytes) − + − + 5 GAS IL-9(lymphocytes) − + − + 5 GAS IL-13 (lymphocyte) − + ? ? 6 GAS IL-15 ? +? + 5 GAS gp140 family IL-3 (myeloid) − − + − 5 GAS(IRF1 > IFP >> Ly6)IL-5 (myeloid) − − + − 5 GAS GM-CSF (myeloid) − − + − 5 GAS Growthhormone family GH ? − + − 5 PRL ? +/− + − 1, 3, 5 EPO ? − + − 5 GAS(B-CAS > IRF1 = IFP >> Ly6) Receptor Tyrosine Kinases EGF ? + + − 1, 3GAS (IRF1) PDGF ? + + − 1, 3 CSF-1 ? + + − 1, 3 GAS(not IRF1)

142 To construct a synthetic GAS containing promoter element, which isused in the Biological Assays described in Examples 78-80, a PCR basedstrategy is employed to generate a GAS-SV40 promoter sequence. The 5′primer contains four tandem copies of the GAS binding site found in theIRF1 promoter and previously demonstrated to bind STATs upon inductionwith a range of cytokines (Rothman et al., Immunity 1:457-468 (1994).),although other GAS or ISRE elements can be used instead. The 5′ primeralso contains 18 bp of sequence complementary to the SV40 early promotersequence and is flanked with an XhoI site. The sequence of the 5′ primeris:

(SEQ ID NO: 1114) 5′:GCGCCTCGAGATTTCCCCGAAATCTAGATTTCCCCGAAATGATTTCCCCGAAATGATTTCCCCGAAATATCTGCCATCTCAATTAG:3′

The downstream primer is complementary to the SV40 promoter and isflanked with a Hind III site: 5′:GCGGCAAGCTTTTTGCAAAGCCTAGGC:3′ (SEQ IDNO: 1115)

PCR amplification is performed using the SV40 promoter template presentin the B-gal:promoter plasmid obtained from Clontech. The resulting PCRfragment is digested with XhoI/Hind III and subcloned into BLSK2−.(Stratagene.) Sequencing with forward and reverse primers confirms thatthe insert contains the following sequence:

(SEQ ID NO: 1116) 5′:CTCGAGATTTCCCCGAAATCTAGATTTCCCCGAAATGATTTCCCCGAAATGATTTCCCCGAAATATCTGCCATCTCAATTAGTCAGCAACCATAGTCCCGCCCCTAACTCCGCCCATCCCGCCCCTAACTCCGCCCAGTTCCGCCCATTCTCCGCCCCATGGCTGACTAATTTTTTTTATTTATGCAGAGGCCGAGGCCGCCTCGGCCTCTGAGCTATTCCAGAAGTAGTGAGGAGGCTTTTTTGGAGGCCTAGGCTTTTGCAAAAAGCTT:3′

With this GAS promoter element linked to the SV40 promoter, a GAS:SEAP2reporter construct is next engineered. Here, the reporter molecule is asecreted alkaline phosphatase, or “SEAP.” Clearly, however, any reportermolecule can be instead of SEAP, in this or in any of the otherExamples. Well known reporter molecules that can be used instead of SEAPinclude chloramphenicol acetyltransferase (CAT), luciferase, alkalinephosphatase, B-galactosidase, green fluorescent protein (GFP), or anyprotein detectable by an antibody.

The above sequence confirmed synthetic GAS-SV40 promoter element issubcloned into the pSEAP-Promoter vector obtained from Clontech usingHindIII and XhoI, effectively replacing the SV40 promoter with theamplified GAS:SV40 promoter element, to create the GAS-SEAP vector.However, this vector does not contain a neomycin resistance gene, andtherefore, is not preferred for mammalian expression systems.

Thus, in order to generate mammalian stable cell lines expressing theGAS-SEAP reporter, the GAS-SEAP cassette is removed from the GAS-SEAPvector using SalI and NotI, and inserted into a backbone vectorcontaining the neomycin resistance gene, such as pGFP-1 (Clontech),using these restriction sites in the multiple cloning site, to createthe GAS-SEAP/Neo vector. Once this vector is transfected into mammaliancells, this vector can then be used as a reporter molecule for GASbinding as described in Examples 78-80.

Other constructs can be made using the above description and replacingGAS with a different promoter sequence. For example, construction ofreporter molecules containing EGR and NF-KB promoter sequences aredescribed in Examples 78-82. However, many other promoters can besubstituted using the protocols described in these Examples. Forinstance, SRE, IL-2, NFAT, or Osteocalcin promoters can be substituted,alone or in combination (e.g., GAS/NF-KB/EGR, GAS/NF-KB, Il-2/NFAT, orNF-KB/GAS). Similarly, other cell lines can be used to test reporterconstruct activity, such as HELA (epithelial), HUVEC (endothelial), Reh(B-cell), Saos-2 (osteoblast), HUVAC (aortic), or Cardiomyocyte.

Example 76 Assay for SEAP Activity

As a reporter molecule for the assays described in examples disclosedherein, SEAP activity is assayed using the Tropix Phospho-light Kit(Cat. BP-400) according to the following general procedure. The TropixPhospho-light Kit supplies the Dilution, Assay, and Reaction Buffersused below.

Prime a dispenser with the 2.5× Dilution Buffer and dispense 15 ul of2.5× dilution buffer into Optiplates containing 35 ul of a solutioncontaining an albumin fusion protein of the invention. Seal the plateswith a plastic sealer and incubate at 65 degree C. for 30 min. Separatethe Optiplates to avoid uneven heating.

Cool the samples to room temperature for 15 minutes. Empty the dispenserand prime with the Assay Buffer. Add 50 ml Assay Buffer and incubate atroom temperature 5 min. Empty the dispenser and prime with the ReactionBuffer (see the Table below). Add 50 ul Reaction Buffer and incubate atroom temperature for 20 minutes. Since the intensity of thechemiluminescent signal is time dependent, and it takes about 10 minutesto read 5 plates on a luminometer, thus one should treat 5 plates ateach time and start the second set 10 minutes later.

Read the relative light unit in the luminometer. Set H12 as blank, andprint the results. An increase in chemiluminescence indicates reporteractivity.

TABLE 6 Rxn buffer # of plates diluent (ml) CSPD (ml) 10 60 3 11 65 3.2512 70 3.5 13 75 3.75 14 80 4 15 85 4.25 16 90 4.5 17 95 4.75 18 100 5 19105 5.25 20 110 5.5 21 115 5.75 22 120 6 23 125 6.25 24 130 6.5 25 1356.75 26 140 7 27 145 7.25 28 150 7.5 29 155 7.75 30 160 8 31 165 8.25 32170 8.5 33 175 8.75 34 180 9 35 185 9.25 36 190 9.5 37 195 9.75 38 20010 39 205 10.25 40 210 10.5 41 215 10.75 42 220 11 43 225 11.25 44 23011.5 45 235 11.75 46 240 12 47 245 12.25 48 250 12.5 49 255 12.75 50 26013

Example 77 Assay Identifying Neuronal Activity

When cells undergo differentiation and proliferation, a group of genesare activated through many different signal transduction pathways. Oneof these genes, EGR1 (early growth response gene 1), is induced invarious tissues and cell types upon activation. The promoter of EGR1 isresponsible for such induction. Using the EGR1 promoter linked toreporter molecules, the ability of fusion proteins of the invention toactivate cells can be assessed.

Particularly, the following protocol is used to assess neuronal activityin PC12 cell lines. PC12 cells (rat phenochromocytoma cells) are knownto proliferate and/or differentiate by activation with a number ofmitogens, such as TPA (tetradecanoyl phorbol acetate), NGF (nerve growthfactor), and EGF (epidermal growth factor). The EGR1 gene expression isactivated during this treatment. Thus, by stably transfecting PC12 cellswith a construct containing an EGR promoter linked to SEAP reporter,activation of PC12 cells by an albumin fusion protein of the presentinvention can be assessed.

The EGR/SEAP reporter construct can be assembled by the followingprotocol. The EGR-1 promoter sequence (−633 to +1)(Sakamoto K et al.,Oncogene 6:867-871 (1991)) can be PCR amplified from human genomic DNAusing the following primers:

First primer: (SEQ ID NO: 1117) 5′ GCGCTCGAGGGATGACAGCGATAGAACCCCGG-3′Second primer: (SEQ ID NO: 1118) 5′ GCGAAGCTTCGCGACTCCCCGGATCCGCCTC-3′

Using the GAS:SEAP/Neo vector produced in Example 75, EGR1 amplifiedproduct can then be inserted into this vector. Linearize theGAS:SEAP/Neo vector using restriction enzymes XhoI/HindIII, removing theGAS/SV40 stuffer. Restrict the EGR1 amplified product with these sameenzymes. Ligate the vector and the EGR1 promoter.

To prepare 96 well-plates for cell culture, two mls of a coatingsolution (1:30 dilution of collagen type I (Upstate Biotech Inc.Cat#08-115) in 30% ethanol (filter sterilized)) is added per one 10 cmplate or 50 ml per well of the 96-well plate, and allowed to air dry for2 hr.

PC12 cells are routinely grown in RPMI-1640 medium (Bio Whittaker)containing 10% horse serum (JRH BIOSCIENCES, Cat. #12449-78P), 5%heat-inactivated fetal bovine serum (FBS) supplemented with 100 units/mlpenicillin and 100 ug/ml streptomycin on a precoated 10 cm tissueculture dish. One to four split is done every three to four days. Cellsare removed from the plates by scraping and resuspended with pipettingup and down for more than 15 times.

Transfect the EGR/SEAP/Neo construct into PC12 using techniques known inthe art. EGR-SEAP/PC12 stable cells are obtained by growing the cells in300 ug/ml G418. The G418-free medium is used for routine growth butevery one to two months, the cells should be re-grown in 300 ug/ml G418for couple of passages.

To assay for neuronal activity, a 10 cm plate with cells around 70 to80% confluent is screened by removing the old medium. Wash the cellsonce with PBS (Phosphate buffered saline). Then starve the cells in lowserum medium (RPMI-1640 containing 1% horse serum and 0.5% FBS withantibiotics) overnight.

The next morning, remove the medium and wash the cells with PBS. Scrapeoff the cells from the plate, suspend the cells well in 2 ml low serummedium. Count the cell number and add more low serum medium to reachfinal cell density as 5×10⁵ cells/ml.

Add 200 ul of the cell suspension to each well of 96-well plate(equivalent to 1×10⁵ cells/well). Add a series of differentconcentrations of an albumin fusion protein of the invention, 37 degreeC. for 48 to 72 hr. As a positive control, a growth factor known toactivate PC12 cells through EGR can be used, such as 50 ng/ul ofNeuronal Growth Factor (NGF). Over fifty-fold induction of SEAP istypically seen in the positive control wells. SEAP assay may beroutinely performed using techniques known in the art and/or asdescribed in Example 76.

Example 78 Assay for T-Cell Activity

The following protocol is used to assess T-cell activity by identifyingfactors, and determining whether an albumin fusion protein of theinvention proliferates and/or differentiates T-cells. T-cell activity isassessed using the GAS/SEAP/Neo construct produced in Example 75. Thus,factors that increase SEAP activity indicate the ability to activate theJaks-STATS signal transduction pathway. The T-cell used in this assay isJurkat T-cells (ATCC Accession No. TIB-152), although Molt-3 cells (ATCCAccession No. CRL-1552) and Molt-4 cells (ATCC Accession No. CRL-1582)cells can also be used.

Jurkat T-cells are lymphoblastic CD4+ Th1 helper cells. In order togenerate stable cell lines, approximately 2 million Jurkat cells aretransfected with the GAS-SEAP/neo vector using DMRIE-C (LifeTechnologies)(transfection procedure described below). The transfectedcells are seeded to a density of approximately 20,000 cells per well andtransfectants resistant to 1 mg/ml genticin selected. Resistant coloniesare expanded and then tested for their response to increasingconcentrations of interferon gamma. The dose response of a selectedclone is demonstrated.

Specifically, the following protocol will yield sufficient cells for 75wells containing 200 ul of cells. Thus, it is either scaled up, orperformed in multiple to generate sufficient cells for multiple 96 wellplates. Jurkat cells are maintained in RPMI+10% serum with 1% Pen-Strep.Combine 2.5 mls of OPTI-MEM (Life Technologies) with 10 ug of plasmidDNA in a T25 flask. Add 2.5 ml OPTI-MEM containing 50 ul of DMRIE-C andincubate at room temperature for 15-45 mins.

During the incubation period, count cell concentration, spin down therequired number of cells (10⁷ per transfection), and resuspend inOPTI-MEM to a final concentration of 10⁷ cells/ml. Then add 1 ml of1×10⁷ cells in OPTI-MEM to T25 flask and incubate at 37 degree C. for 6hrs. After the incubation, add 10 ml of RPMI+15% serum.

The Jurkat:GAS-SEAP stable reporter lines are maintained in RPMI+10%serum, 1 mg/ml Genticin, and 1% Pen-Strep. These cells are treated withvarying concentrations of one or more fusion proteins of the presentinvention.

On the day of treatment with the fusion protein, the cells should bewashed and resuspended in fresh RPMI+10% serum to a density of 500,000cells per ml. The exact number of cells required will depend on thenumber of fusion proteins and the number of different concentrations offusion proteins being screened. For one 96 well plate, approximately 10million cells (for 10 plates, 100 million cells) are required.

The well dishes containing Jurkat cells treated with the fusion proteinare placed in an incubator for 48 hrs (note: this time is variablebetween 48-72 hrs). 35 ul samples from each well are then transferred toan opaque 96 well plate using a 12 channel pipette. The opaque platesshould be covered (using sellophene covers) and stored at −20 degree C.until SEAP assays are performed according to Example 76. The platescontaining the remaining treated cells are placed at 4 degree C. andserve as a source of material for repeating the assay on a specific wellif desired.

As a positive control, 100 Unit/ml interferon gamma can be used which isknown to activate Jurkat T cells. Over 30 fold induction is typicallyobserved in the positive control wells.

The above protocol may be used in the generation of both transient, aswell as, stable transfected cells, which would be apparent to those ofskill in the art.

Example 79 Assay for T-Cell Activity

NF-KB (Nuclear Factor KB) is a transcription factor activated by a widevariety of agents including the inflammatory cytokines IL-1 and TNF,CD30 and CD40, lymphotoxin-alpha and lymphotoxin-beta, by exposure toLPS or thrombin, and by expression of certain viral gene products. As atranscription factor, NF-KB regulates the expression of genes involvedin immune cell activation, control of apoptosis (NF-KB appears to shieldcells from apoptosis), B and T-cell development, anti-viral andantimicrobial responses, and multiple stress responses.

In non-stimulated conditions, NF-KB is retained in the cytoplasm withI-KB (Inhibitor KB). However, upon stimulation, I-KB is phosphorylatedand degraded, causing NF-KB to shuttle to the nucleus, therebyactivating transcription of target genes. Target genes activated byNF-KB include IL-2, IL-6, GM-CSF, ICAM-1 and class 1 MHC.

Due to its central role and ability to respond to a range of stimuli,reporter constructs utilizing the NF-KB promoter element are used toscreen the fusion protein. Activators or inhibitors of NF-KB would beuseful in treating, preventing, and/or diagnosing diseases. For example,inhibitors of NF-KB could be used to treat those diseases related to theacute or chronic activation of NF-KB, such as rheumatoid arthritis.

To construct a vector containing the NF-KB promoter element, a PCR basedstrategy is employed. The upstream primer contains four tandem copies ofthe NF-KB binding site (GGGGACTTTCCC) (SEQ ID NO: 1119), 18 bp ofsequence complementary to the 5′ end of the SV40 early promotersequence, and is flanked with an XhoI site:

(SEQ ID NO: 1120) 5′:GCGGCCTCGAGGGGACTTTCCCGGGGACTTTCCGGGGACTTTCCGGGACTTTCCATCCTGCCATCTCAATTAG:3′

The downstream primer is complementary to the 3′ end of the SV40promoter and is flanked with a Hind III site:

(SEQ ID NO: 1115) 5′:GCGGCAAGCTTTTTGCAAAGCCTAGGC:3′

PCR amplification is performed using the SV40 promoter template presentin the pB-gal:promoter plasmid obtained from Clontech. The resulting PCRfragment is digested with XhoI and Hind III and subcloned into BLSK2−.(Stratagene) Sequencing with the T7 and T3 primers confirms the insertcontains the following sequence:

(SEQ ID NO: 1121) 5′:CTCGAGGGGACTTTCCCGGGGACTTTCCGGGGACTTTCCGGGACTTTCCATCTGCCATCTCAATTAGTCAGCAACCATAGTCCCGCCCCTAACTCCGCCCATCCCGCCCCTAACTCCGCCCAGTTCCGCCCATTCTCCGCCCCATGGCTGACTAATTTTTTTTATTTATGCAGAGGCCGAGGCCGCCTCGGCCTCTGAGCTATTCCAGAAGTAGTGAGGAGGCTTTTTTGGAGGCCTAGGCTTTTGC AAAAAGCTT:3′

Next, replace the SV40 minimal promoter element present in thepSEAP2-promoter plasmid (Clontech) with this NF-KB/SV40 fragment usingXhoI and HindIII. However, this vector does not contain a neomycinresistance gene, and therefore, is not preferred for mammalianexpression systems.

In order to generate stable mammalian cell lines, the NF-KB/SV40/SEAPcassette is removed from the above NF-KB/SEAP vector using restrictionenzymes SalI and NotI, and inserted into a vector containing neomycinresistance. Particularly, the NF-KB/SV40/SEAP cassette was inserted intopGFP-1 (Clontech), replacing the GFP gene, after restricting pGFP-1 withSalI and NotI.

Once NF-KB/SV40/SEAP/Neo vector is created, stable Jurkat T-cells arecreated and maintained according to the protocol described in Example76. Similarly, the method for assaying fusion proteins with these stableJurkat T-cells is also described in Example 76. As a positive control,exogenous TNF alpha (0.1, 1, 10 ng) is added to wells H9, H10, and H11,with a 5-10 fold activation typically observed.

Example 80 Assay Identifying Myeloid Activity

The following protocol is used to assess myeloid activity of an albuminfusion protein of the present invention by determining whether thefusion protein proliferates and/or differentiates myeloid cells. Myeloidcell activity is assessed using the GAS/SEAP/Neo construct produced inExample 75. Thus, factors that increase SEAP activity indicate theability to activate the Jaks-STATS signal transduction pathway. Themyeloid cell used in this assay is U937, a pre-monocyte cell line,although TF-1, HL60, or KG1 can be used.

To transiently transfect U937 cells with the GAS/SEAP/Neo constructproduced in Example 75, a DEAE-Dextran method (Kharbanda et. al., 1994,Cell Growth & Differentiation, 5:259-265) is used. First, harvest 2×10⁷U937 cells and wash with PBS. The U937 cells are usually grown in RPMI1640 medium containing 10% heat-inactivated fetal bovine serum (FBS)supplemented with 100 units/ml penicillin and 100 mg/ml streptomycin.

Next, suspend the cells in 1 ml of 20 mM Tris-HCl (pH 7.4) buffercontaining 0.5 mg/ml DEAE-Dextran, 8 ug GAS-SEAP2 plasmid DNA, 140 mMNaCl, 5 mM KCl, 375 uM Na₂HPO₄.7H₂O, 1 mM MgCl₂, and 675 uM CaCl₂.Incubate at 37 degrees C. for 45 min.

Wash the cells with RPMI 1640 medium containing 10% FBS and thenresuspend in 10 ml complete medium and incubate at 37 degree C. for 36hr.

The GAS-SEAP/U937 stable cells are obtained by growing the cells in 400ug/ml G418. The G418-free medium is used for routine growth but everyone to two months, the cells should be re-grown in 400 ug/ml G418 forcouple of passages.

These cells are tested by harvesting 110⁸ cells (this is enough for ten96-well plates assay) and wash with PBS. Suspend the cells in 200 mlabove described growth medium, with a final density of 5×10⁵ cells/ml.Plate 200 ul cells per well in the 96-well plate (or 1×10⁵ cells/well).

Add different concentrations of the fusion protein. Incubate at 37degree C. for 48 to 72 hr. As a positive control, 100 Unit/ml interferongamma can be used which is known to activate U937 cells. Over 30 foldinduction is typically observed in the positive control wells. SEAPassay the supernatant according to methods known in the art and/or theprotocol described in Example 76.

Example 81 Assay Identifying Changes in Small Molecule Concentration andMembrane Permeability

Binding of a ligand to a receptor is known to alter intracellular levelsof small molecules, such as calcium, potassium, sodium, and pH, as wellas alter membrane potential. These alterations can be measured in anassay to identify fusion proteins which bind to receptors of aparticular cell. Although the following protocol describes an assay forcalcium, this protocol can easily be modified to detect changes inpotassium, sodium, pH, membrane potential, or any other small moleculewhich is detectable by a fluorescent probe.

The following assay uses Fluorometric Imaging Plate Reader (“FLIPR”) tomeasure changes in fluorescent molecules (Molecular Probes) that bindsmall molecules. Clearly, any fluorescent molecule detecting a smallmolecule can be used instead of the calcium fluorescent molecule, fluo-4(Molecular Probes, Inc.; catalog no. F-14202), used here.

For adherent cells, seed the cells at 10,000-20,000 cells/well in aCo-star black 96-well plate with clear bottom. The plate is incubated ina CO₂ incubator for 20 hours. The adherent cells are washed two times inBiotek washer with 200 ul of HBSS (Hank's Balanced Salt Solution)leaving 100 ul of buffer after the final wash.

A stock solution of 1 mg/ml fluo-4 is made in 10% pluronic acid DMSO. Toload the cells with fluo-4, 50 ul of 12 ug/ml fluo-4 is added to eachwell. The plate is incubated at 37 degrees C. in a CO₂ incubator for 60min. The plate is washed four times in the Biotek washer with HBSSleaving 100 ul of buffer.

For non-adherent cells, the cells are spun down from culture media.Cells are re-suspended to 2-5×10⁶ cells/ml with HBSS in a 50-ml conicaltube. 4 ul of 1 mg/ml fluo-4 solution in 10% pluronic acid DMSO is addedto each ml of cell suspension. The tube is then placed in a 37 degreesC. water bath for 30-60 min. The cells are washed twice with HBSS,resuspended to 1×10⁶ cells/ml, and dispensed into a microplate, 100ul/well. The plate is centrifuged at 1000 rpm for 5 min. The plate isthen washed once in Denley Cell Wash with 200 ul, followed by anaspiration step to 100 ul final volume.

For a non-cell based assay, each well contains a fluorescent molecule,such as fluo-4. The fusion protein of the invention is added to thewell, and a change in fluorescence is detected.

To measure the fluorescence of intracellular calcium, the FLIPR is setfor the following parameters: (1) System gain is 300-800 mW; (2)Exposure time is 0.4 second; (3) Camera F/stop is F/2; (4) Excitation is488 nm; (5) Emission is 530 nm; and (6) Sample addition is 50 ul.Increased emission at 530 nm indicates an extracellular signaling eventcaused by an albumin fusion protein of the present invention or amolecule induced by an albumin fusion protein of the present invention,which has resulted in an increase in the intracellular Ca⁺⁺concentration.

Example 82 Assay Identifying Tyrosine Kinase Activity

The Protein Tyrosine Kinases (PTK) represent a diverse group oftransmembrane and cytoplasmic kinases. Within the Receptor ProteinTyrosine Kinase (RPTK) group are receptors for a range of mitogenic andmetabolic growth factors including the PDGF, FGF, EGF, NGF, HGF andInsulin receptor subfamilies. In addition there are a large family ofRPTKs for which the corresponding ligand is unknown. Ligands for RPTKsinclude mainly secreted small proteins, but also membrane-bound andextracellular matrix proteins.

Activation of RPTK by ligands involves ligand-mediated receptordimerization, resulting in transphosphorylation of the receptor subunitsand activation of the cytoplasmic tyrosine kinases. The cytoplasmictyrosine kinases include receptor associated tyrosine kinases of thesrc-family (e.g., src, yes, lck, lyn, fyn) and non-receptor linked andcytosolic protein tyrosine kinases, such as the Jak family, members ofwhich mediate signal transduction triggered by the cytokine superfamilyof receptors (e.g., the Interleukins, Interferons, GM-CSF, and Leptin).

Because of the wide range of known factors capable of stimulatingtyrosine kinase activity, identifying whether an albumin fusion proteinof the present invention or a molecule induced by a fusion protein ofthe present invention is capable of activating tyrosine kinase signaltransduction pathways is of interest. Therefore, the following protocolis designed to identify such molecules capable of activating thetyrosine kinase signal transduction pathways.

Seed target cells (e.g., primary keratinocytes) at a density ofapproximately 25,000 cells per well in a 96 well Loprodyne Silent ScreenPlates purchased from Nalge Nunc (Naperville, Ill.). The plates aresterilized with two 30 minute rinses with 100% ethanol, rinsed withwater and dried overnight. Some plates are coated for 2 hr with 100 mlof cell culture grade type I collagen (50 mg/ml), gelatin (2%) orpolylysine (50 mg/ml), all of which can be purchased from SigmaChemicals (St. Louis, Mo.) or 10% Matrigel purchased from BectonDickinson (Bedford, Mass.), or calf serum, rinsed with PBS and stored at4 degree C. Cell growth on these plates is assayed by seeding 5,000cells/well in growth medium and indirect quantitation of cell numberthrough use of alamarBlue as described by the manufacturer AlamarBiosciences, Inc. (Sacramento, Calif.) after 48 hr. Falcon plate covers#3071 from Becton Dickinson (Bedford, Mass.) are used to cover theLoprodyne Silent Screen Plates. Falcon Microtest III cell culture platescan also be used in some proliferation experiments.

To prepare extracts, A431 cells are seeded onto the nylon membranes ofLoprodyne plates (20,000/200 ml/well) and cultured overnight in completemedium. Cells are quiesced by incubation in serum-free basal medium for24 hr. After 5-20 minutes treatment with EGF (60 ng/ml) or a differentconcentrations of an albumin fusion protein of the invention, the mediumwas removed and 100 ml of extraction buffer ((20 mM HEPES pH 7.5, 0.15 MNaCl, 1% Triton X-100, 0.1% SDS, 2 mM Na3VO4, 2 mM Na4P2O7 and acocktail of protease inhibitors (#1836170) obtained from BoeheringerMannheim (Indianapolis, Ind.)) is added to each well and the plate isshaken on a rotating shaker for 5 minutes at 4° C. The plate is thenplaced in a vacuum transfer manifold and the extract filtered throughthe 0.45 mm membrane bottoms of each well using house vacuum. Extractsare collected in a 96-well catch/assay plate in the bottom of the vacuummanifold and immediately placed on ice. To obtain extracts clarified bycentrifugation, the content of each well, after detergent solubilizationfor 5 minutes, is removed and centrifuged for 15 minutes at 4 degree C.at 16,000×g.

Test the filtered extracts for levels of tyrosine kinase activity.Although many methods of detecting tyrosine kinase activity are known,one method is described here.

Generally, the tyrosine kinase activity of an albumin fusion protein ofthe invention is evaluated by determining its ability to phosphorylate atyrosine residue on a specific substrate (a biotinylated peptide).Biotinylated peptides that can be used for this purpose include PSK1(corresponding to amino acids 6-20 of the cell division kinase cdc2-p34)and PSK2 (corresponding to amino acids 1-17 of gastrin). Both peptidesare substrates for a range of tyrosine kinases and are available fromBoehringer Mannheim.

The tyrosine kinase reaction is set up by adding the followingcomponents in order. First, add 10 ul of 5 uM Biotinylated Peptide, then10 ul ATP/Mg₂₊ (5 mM ATP/50 mM MgCl₂), then 10 ul of 5× Assay Buffer (40mM imidazole hydrochloride, pH7.3, 40 mM beta-glycerophosphate, 1 mMEGTA, 100 mM MgCl₂, 5 mM MnCl₂, 0.5 mg/ml BSA), then 5 ul of SodiumVanadate (1 mM), and then 5 ul of water. Mix the components gently andpreincubate the reaction mix at 30 degree C. for 2 min. Initial thereaction by adding 10 ul of the control enzyme or the filteredsupernatant.

The tyrosine kinase assay reaction is then terminated by adding 10 ul of120 mm EDTA and place the reactions on ice.

Tyrosine kinase activity is determined by transferring 50 ul aliquot ofreaction mixture to a microtiter plate (MTP) module and incubating at 37degree C. for 20 min. This allows the streptavidin coated 96 well plateto associate with the biotinylated peptide. Wash the MTP module with 300ul/well of PBS four times. Next add 75 ul of anti-phospotyrosineantibody conjugated to horse radish peroxidase (anti-P-Tyr-POD(0.5u/ml)) to each well and incubate at 37 degree C. for one hour. Wash thewell as above.

Next add 100 ul of peroxidase substrate solution (Boehringer Mannheim)and incubate at room temperature for at least 5 mins (up to 30 min).Measure the absorbance of the sample at 405 nm by using ELISA reader.The level of bound peroxidase activity is quantitated using an ELISAreader and reflects the level of tyrosine kinase activity.

Example 83 Assay Identifying Phosphorylation Activity

As a potential alternative and/or complement to the assay of proteintyrosine kinase activity described in Example 82, an assay which detectsactivation (phosphorylation) of major intracellular signal transductionintermediates can also be used. For example, as described below oneparticular assay can detect tyrosine phosphorylation of the Erk-1 andErk-2 kinases. However, phosphorylation of other molecules, such as Raf,JNK, p38 MAP, Map kinase kinase (MEK), MEK kinase, Src, Muscle specifickinase (MuSK), IRAK, Tec, and Janus, as well as any other phosphoserine,phosphotyrosine, or phosphothreonine molecule, can be detected bysubstituting these molecules for Erk-1 or Erk-2 in the following assay.

Specifically, assay plates are made by coating the wells of a 96-wellELISA plate with 0.1 ml of protein G (1 ug/ml) for 2 hr at room temp,(RT). The plates are then rinsed with PBS and blocked with 3% BSA/PBSfor 1 hr at RT. The protein G plates are then treated with 2 commercialmonoclonal antibodies (100 ng/well) against Erk-1 and Erk-2 (1 hr at RT)(Santa Cruz Biotechnology). (To detect other molecules, this step caneasily be modified by substituting a monoclonal antibody detecting anyof the above described molecules.) After 3-5 rinses with PBS, the platesare stored at 4 degree C. until use.

A431 cells are seeded at 20,000/well in a 96-well Loprodyne filterplateand cultured overnight in growth medium. The cells are then starved for48 hr in basal medium (DMEM) and then treated with EGF (6 ng/well) orvarying concentrations of the fusion protein of the invention for 5-20minutes. The cells are then solubilized and extracts filtered directlyinto the assay plate.

After incubation with the extract for 1 hr at RT, the wells are againrinsed. As a positive control, a commercial preparation of MAP kinase(10 ng/well) is used in place of A431 extract. Plates are then treatedwith a commercial polyclonal (rabbit) antibody (1 ug/ml) whichspecifically recognizes the phosphorylated epitope of the Erk-1 andErk-2 kinases (1 hr at RT). This antibody is biotinylated by standardprocedures. The bound polyclonal antibody is then quantitated bysuccessive incubations with Europium-streptavidin and Europiumfluorescence enhancing reagent in the Wallac DELFIA instrument(time-resolved fluorescence). An increased fluorescent signal overbackground indicates a phosphorylation by the fusion protein of thepresent invention or a molecule induced by an albumin fusion protein ofthe present invention.

Example 84 Assay for the Stimulation of Bone Marrow CD34+ CellProliferation

This assay is based on the ability of human CD34+ to proliferate in thepresence of hematopoietic growth factors and evaluates the ability offusion proteins of the invention to stimulate proliferation of CD34+cells.

It has been previously shown that most mature precursors will respond toonly a single signal. More immature precursors require at least twosignals to respond. Therefore, to test the effect of fusion proteins ofthe invention on hematopoietic activity of a wide range of progenitorcells, the assay contains a given fusion protein of the invention in thepresence or absence of hematopoietic growth factors. Isolated cells arecultured for 5 days in the presence of Stem Cell Factor (SCF) incombination with tested sample. SCF alone has a very limited effect onthe proliferation of bone marrow (BM) cells, acting in such conditionsonly as a “survival” factor. However, combined with any factorexhibiting stimulatory effect on these cells (e.g., IL-3), SCF willcause a synergistic effect. Therefore, if the tested fusion protein hasa stimulatory effect on hematopoietic progenitors, such activity can beeasily detected. Since normal BM cells have a low level of cyclingcells, it is likely that any inhibitory effect of a given fusion proteinmight not be detected. Accordingly, assays for an inhibitory effect onprogenitors is preferably tested in cells that are first subjected to invitro stimulation with SCF+IL+3, and then contacted with the compoundthat is being evaluated for inhibition of such induced proliferation.

Briefly, CD34+ cells are isolated using methods known in the art. Thecells are thawed and resuspended in medium (QBSF 60 serum-free mediumwith 1% L-glutamine (500 ml) Quality Biological, Inc., Gaithersburg, Md.Cat#160-204-101). After several gentle centrifugation steps at 200×g,cells are allowed to rest for one hour. The cell count is adjusted to2.5×10⁵ cells/ml. During this time, 100 μl of sterile water is added tothe peripheral wells of a 96-well plate. The cytokines that can betested with an albumin fusion protein of the invention in this assay isrhSCF (R&D Systems, Minneapolis, Minn., Cat#255-SC) at 50 ng/ml aloneand in combination with rhSCF and rhIL-3 (R&D Systems, Minneapolis,Minn., Cat#203-ML) at 30 ng/ml. After one hour, 10 μl of preparedcytokines, varying concentrations of an albumin fusion protein of theinvention, and 20 μl of diluted cells are added to the media which isalready present in the wells to allow for a final total volume of 100The plates are then placed in a 37° C./5% CO₂ incubator for five days.

Eighteen hours before the assay is harvested, 0.5 μCi/well of [3H]Thymidine is added in a 10 μl volume to each well to determine theproliferation rate. The experiment is terminated by harvesting the cellsfrom each 96-well plate to a filtermat using the Tomtec Harvester 96.After harvesting, the filtermats are dried, trimmed and placed intoOmniFilter assemblies consisting of one OmniFilter plate and oneOmniFilter Tray. 60 μl Microscint is added to each well and the platesealed with TopSeal-A press-on sealing film A bar code 15 sticker isaffixed to the first plate for counting. The sealed plates are thenloaded and the level of radioactivity determined via the Packard TopCount and the printed data collected for analysis. The level ofradioactivity reflects the amount of cell proliferation.

The studies described in this example test the activity of a givenfusion protein to stimulate bone marrow CD34+ cell proliferation. Oneskilled in the art could easily modify the exemplified studies to testthe activity of fusion proteins and polynucleotides of the invention(e.g., gene therapy) as well as agonists and antagonists thereof. Theability of an albumin fusion protein of the invention to stimulate theproliferation of bone marrow CD34+ cells indicates that the albuminfusion protein and/or polynucleotides corresponding to the fusionprotein are useful for the diagnosis and treatment of disordersaffecting the immune system and hematopoiesis. Representative uses aredescribed in the “Immune Activity” and “Infectious Disease” sectionsabove, and elsewhere herein.

Example 85 Assay for Extracellular Matrix Enhanced Cell Response (EMECR)

The objective of the Extracellular Matrix Enhanced Cell Response (EMECR)assay is to evaluate the ability of fusion proteins of the invention toact on hematopoietic stem cells in the context of the extracellularmatrix (ECM) induced signal.

Cells respond to the regulatory factors in the context of signal(s)received from the surrounding microenvironment. For example,fibroblasts, and endothelial and epithelial stem cells fail to replicatein the absence of signals from the ECM. Hematopoietic stem cells canundergo self-renewal in the bone marrow, but not in in vitro suspensionculture. The ability of stem cells to undergo self-renewal in vitro isdependent upon their interaction with the stromal cells and the ECMprotein fibronectin (fn). Adhesion of cells to fn is mediated by theα₅.β₁ and α₄.β₁ integrin receptors, which are expressed by human andmouse hematopoietic stem cells. The factor(s) which integrate with theECM environment and are responsible for stimulating stem cellself-renewal have not yet been identified. Discovery of such factorsshould be of great interest in gene therapy and bone marrow transplantapplications

Briefly, polystyrene, non tissue culture treated, 96-well plates arecoated with fn fragment at a coating concentration of 0.2 μg/cm². Mousebone marrow cells are plated (1,000 cells/well) in 0.2 ml of serum-freemedium. Cells cultured in the presence of IL-3 (5 ng/ml)+SCF (50 ng/ml)would serve as the positive control, conditions under which littleself-renewal but pronounced differentiation of the stem cells is to beexpected. Albumin fusion proteins of the invention are tested withappropriate negative controls in the presence and absence of SCF (5.0ng/ml), where volume of the administered composition containing thealbumin fusion protein of the invention represents 10% of the totalassay volume. The plated cells are then allowed to grow by incubating ina low oxygen environment (5% CO₂, 7% O₂, and 88% N₂) tissue cultureincubator for 7 days. The number of proliferating cells within the wellsis then quantitated by measuring thymidine incorporation into cellularDNA. Verification of the positive hits in the assay will requirephenotypic characterization of the cells, which can be accomplished byscaling up of the culture system and using appropriate antibody reagentsagainst cell surface antigens and FAC Scan.

If a particular fusion protein of the present invention is found to be astimulator of hematopoietic progenitors, the fusion protein andpolynucleotides corresponding to the fusion protein may be useful forexample, in the diagnosis and treatment of disorders affecting theimmune system and hematopoiesis. Representative uses are described inthe “Immune Activity” and “Infectious Disease” sections above, andelsewhere herein. The fusion protein may also be useful in the expansionof stem cells and committed progenitors of various blood lineages, andin the differentiation and/or proliferation of various cell types.

Additionally, the albumin fusion proteins of the invention andpolynucleotides encoding albumin fusion proteins of the invention, mayalso be employed to inhibit the proliferation and differentiation ofhematopoietic cells and therefore may be employed to protect bone marrowstem cells from chemotherapeutic agents during chemotherapy. Thisantiproliferative effect may allow administration of higher doses ofchemotherapeutic agents and, therefore, more effective chemotherapeutictreatment.

Moreover, fusion proteins of the invention and polynucleotides encodingalbumin fusion proteins of the invention may also be useful for thetreatment and diagnosis of hematopoietic related disorders such as,anemia, pancytopenia, leukopenia, thrombocytopenia or leukemia, sincestromal cells are important in the production of cells of hematopoieticlineages. The uses include bone marrow cell ex-vivo culture, bone marrowtransplantation, bone marrow reconstitution, radiotherapy orchemotherapy of neoplasia.

Example 86 Human Dermal Fibroblast and Aortic Smooth Muscle CellProliferation

An albumin fusion protein of the invention is added to cultures ofnormal human dermal fibroblasts (NHDF) and human aortic smooth musclecells (AoSMC) and two co-assays are performed with each sample. Thefirst assay examines the effect of the fusion protein on theproliferation of normal human dermal fibroblasts (NHDF) or aortic smoothmuscle cells (AoSMC). Aberrant growth of fibroblasts or smooth musclecells is a part of several pathological processes, including fibrosis,and restenosis. The second assay examines IL6 production by both NHDFand SMC. IL6 production is an indication of functional activation.Activated cells will have increased production of a number of cytokinesand other factors, which can result in a proinflammatory orimmunomodulatory outcome. Assays are run with and without co-TNFastimulation, in order to check for costimulatory or inhibitory activity.

Briefly, on day 1, 96-well black plates are set up with 1000 cells/well(NHDF) or 2000 cells/well (AoSMC) in 100 μl culture media. NHDF culturemedia contains: Clonetics FB basal media, 1 mg/ml hFGF, 5 mg/ml insulin,50 mg/ml gentamycin, 2% FBS, while AoSMC culture media containsClonetics SM basal media, 0.5 μg/ml hEGF, 5 mg/ml insulin, 1 μg/ml hFGF,50 mg/ml gentamycin, 50 μg/ml Amphotericin B, 5% FBS. After incubationat 37° C. for at least 4-5 hours culture media is aspirated and replacedwith growth arrest media. Growth arrest media for NHDF containsfibroblast basal media, 50 mg/ml gentamycin, 2% FBS, while growth arrestmedia for AoSMC contains SM basal media, 50 mg/ml gentamycin, 50 μg/mlAmphotericin B, 0.4% FBS. Incubate at 37° C. until day 2.

On day 2, serial dilutions and templates of an albumin fusion protein ofthe invention are designed such that they always include media controlsand known-protein controls. For both stimulation and inhibitionexperiments, proteins are diluted in growth arrest media. For inhibitionexperiments, TNFa is added to a final concentration of 2 ng/ml (NHDF) or5 ng/ml (AoSMC). Add 1/3 vol media containing controls or an albuminfusion protein of the invention and incubate at 37 degrees C./5% CO₂until day 5.

Transfer 60 μl from each well to another labeled 96-well plate, coverwith a plate-sealer, and store at 4 degrees C. until Day 6 (for IL6ELISA). To the remaining 100 μl in the cell culture plate, asepticallyadd Alamar Blue in an amount equal to 10% of the culture volume (10 μl).Return plates to incubator for 3 to 4 hours. Then measure fluorescencewith excitation at 530 nm and emission at 590 nm using the CytoFluor.This yields the growth stimulation/inhibition data.

On day 5, the IL6 ELISA is performed by coating a 96 well plate with50-100 ul/well of Anti-Human IL6 Monoclonal antibody diluted in PBS, pH7.4, incubate ON at room temperature.

On day 6, empty the plates into the sink and blot on paper towels.Prepare Assay Buffer containing PBS with 4% BSA. Block the plates with200 μl/well of Pierce Super Block blocking buffer in PBS for 1-2 hr andthen wash plates with wash buffer (PBS, 0.05% Tween-20). Blot plates onpaper towels. Then add 50 μl/well of diluted Anti-Human IL-6 Monoclonal,Biotin-labeled antibody at 0.50 mg/ml. Make dilutions of IL-6 stock inmedia (30, 10, 3, 1, 0.3, 0 ng/ml). Add duplicate samples to top row ofplate. Cover the plates and incubate for 2 hours at RT on shaker.

Plates are washed with wash buffer and blotted on paper towels. DiluteEU-labeled Streptavidin 1:1000 in Assay buffer, and add 100 μl/well.Cover the plate and incubate 1 h at RT. Plates are again washed withwash buffer and blotted on paper towels.

Add 100 μl/well of Enhancement Solution. Shake for 5 minutes. Read theplate on the Wallac DELFIA Fluorometer. Readings from triplicate samplesin each assay were tabulated and averaged.

A positive result in this assay suggests AoSMC cell proliferation andthat the albumin fusion protein may be involved in dermal fibroblastproliferation and/or smooth muscle cell proliferation. A positive resultalso suggests many potential uses of the fusion protein andpolynucleotides encoding the albumin fusion protein. For example,inflammation and immune responses, wound healing, and angiogenesis, asdetailed throughout this specification. Particularly, fusion proteinsmay be used in wound healing and dermal regeneration, as well as thepromotion of vasculogenesis, both of the blood vessels and lymphatics.The growth of vessels can be used in the treatment of, for example,cardiovascular diseases. Additionally, fusion proteins showingantagonistic activity in this assay may be useful in treating diseases,disorders, and/or conditions which involve angiogenesis by acting as ananti-vascular agent (e.g., anti-angiogenesis). These diseases,disorders, and/or conditions are known in the art and/or are describedherein, such as, for example, malignancies, solid tumors, benign tumors,for example hemangiomas, acoustic neuromas, neurofibromas, trachomas,and pyogenic granulomas; artheroscleric plaques; ocular angiogenicdiseases, for example, diabetic retinopathy, retinopathy of prematurity,macular degeneration, corneal graft rejection, neovascular glaucoma,retrolental fibroplasia, rubeosis, retinoblastoma, uvietis and Pterygia(abnormal blood vessel growth) of the eye; rheumatoid arthritis;psoriasis; delayed wound healing; endometriosis; vasculogenesis;granulations; hypertrophic scars (keloids); nonunion fractures;scleroderma; trachoma; vascular adhesions; myocardial angiogenesis;coronary collaterals; cerebral collaterals; arteriovenous malformations;ischemic limb angiogenesis; Osler-Webber Syndrome; plaqueneovascularization; telangiectasia; hemophiliac joints; angiofibroma;fibromuscular dysplasia; wound granulation; Crohn's disease; andatherosclerosis. Moreover, albumin fusion proteins that act asantagonists in this assay may be useful in treatinganti-hyperproliferative diseases and/or anti-inflammatory known in theart and/or described herein.

Example 87 Cellular Adhesion Molecule (CAM) Expression on EndothelialCells

The recruitment of lymphocytes to areas of inflammation and angiogenesisinvolves specific receptor-ligand interactions between cell surfaceadhesion molecules (CAMs) on lymphocytes and the vascular endothelium.The adhesion process, in both normal and pathological settings, followsa multi-step cascade that involves intercellular adhesion molecule-1(ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and endothelialleukocyte adhesion molecule-1 (E-selectin) expression on endothelialcells (EC). The expression of these molecules and others on the vascularendothelium determines the efficiency with which leukocytes may adhereto the local vasculature and extravasate into the local tissue duringthe development of an inflammatory response. The local concentration ofcytokines and growth factor participate in the modulation of theexpression of these CAMs.

Briefly, endothelial cells (e.g., Human Umbilical Vein Endothelial cells(HUVECs)) are grown in a standard 96 well plate to confluence, growthmedium is removed from the cells and replaced with 100 μl of 199 Medium(10% fetal bovine serum (FBS)). Samples for testing (containing analbumin fusion protein of the invention) and positive or negativecontrols are added to the plate in triplicate (in 10 μl volumes). Platesare then incubated at 37° C. for either 5 h (selectin and integrinexpression) or 24 h (integrin expression only). Plates are aspirated toremove medium and 100 μl of 0.1% paraformaldehyde-PBS (with Ca++ andMg++) is added to each well. Plates are held at 4° C. for 30 min.Fixative is removed from the wells and wells are washed 1× withPBS(+Ca,Mg)+0.5% BSA and drained. 10 μl of diluted primary antibody isadded to the test and control wells. Anti-ICAM-1-Biotin,Anti-VCAM-1-Biotin and Anti-E-selectin-Biotin are used at aconcentration of 10 μg/ml (1:10 dilution of 0.1 mg/ml stock antibody).Cells are incubated at 37° C. for 30 min. in a humidified environment.Wells are washed three times with PBS(+Ca,Mg)+0.5% BSA. 20 μl of dilutedExtrAvidin-Alkaline Phosphatase (1:5,000 dilution, referred to herein asthe working dilution) are added to each well and incubated at 37° C. for30 min. Wells are washed three times with PBS(+Ca,Mg)+0.5% BSA. Dissolve1 tablet of p-Nitrophenol Phosphate pNPP per 5 ml of glycine buffer (pH10.4). 100 μl of pNPP substrate in glycine buffer is added to each testwell. Standard wells in triplicate are prepared from the workingdilution of the ExtrAvidin-Alkaline Phosphotase in glycine buffer:1:5,000) (10⁰)>10^(−0.5)>10⁻¹>10^(−1.5). 5 μl of each dilution is addedto triplicate wells and the resulting AP content in each well is 5.50ng, 1.74 ng, 0.55 ng, 0.18 ng. 100 μl of pNNP reagent is then added toeach of the standard wells. The plate is incubated at 37° C. for 4 h. Avolume of 50 μl of 3M NaOH is added to all wells. The plate is read on aplate reader at 405 nm using the background subtraction option on blankwells filled with glycine buffer only. Additionally, the template is setup to indicate the concentration of AP-conjugate in each standard well[5.50 ng; 1.74 ng; 0.55 ng; 0.18 ng]. Results are indicated as amount ofbound AP-conjugate in each sample.

Example 88 Alamar Blue Endothelial Cells Proliferation Assay

This assay may be used to quantitatively determine protein mediatedinhibition of bFGF-induced proliferation of Bovine Lymphatic EndothelialCells (LECs), Bovine Aortic Endothelial Cells (BAECs) or HumanMicrovascular Uterine Myometrial Cells (UTMECs). This assay incorporatesa fluorometric growth indicator based on detection of metabolicactivity. A standard Alamar Blue Proliferation Assay is prepared inEGM-2MV with 10 ng/ml of bFGF added as a source of endothelial cellstimulation. This assay may be used with a variety of endothelial cellswith slight changes in growth medium and cell concentration. Dilutionsof protein batches to be tested are diluted as appropriate. Serum-freemedium (GIBCO SFM) without bFGF is used as a non-stimulated control andAngiostatin or TSP-1 are included as a known inhibitory controls.

Briefly, LEC, BAECs or UTMECs are seeded in growth media at a density of5000 to 2000 cells/well in a 96 well plate and placed at 37 degrees C.overnight. After the overnight incubation of the cells, the growth mediais removed and replaced with GIBCO EC-SFM. The cells are treated withthe appropriate dilutions of an albumin fusion protein of the inventionor control protein sample(s) (prepared in SFM) in triplicate wells withadditional bFGF to a concentration of 10 ng/ml. Once the cells have beentreated with the samples, the plate(s) is/are placed back in the 37° C.incubator for three days. After three days 10 ml of stock alamar blue(Biosource Cat# DAL1100) is added to each well and the plate(s) is/areplaced back in the 37° C. incubator for four hours. The plate(s) arethen read at 530 nm excitation and 590 nm emission using the CytoFluorfluorescence reader. Direct output is recorded in relative fluorescenceunits.

Alamar blue is an oxidation-reduction indicator that both fluoresces andchanges color in response to chemical reduction of growth mediumresulting from cell growth. As cells grow in culture, innate metabolicactivity results in a chemical reduction of the immediate surroundingenvironment. Reduction related to growth causes the indicator to changefrom oxidized (non-fluorescent blue) form to reduced (fluorescent red)form (i.e., stimulated proliferation will produce a stronger signal andinhibited proliferation will produce a weaker signal and the totalsignal is proportional to the total number of cells as well as theirmetabolic activity). The background level of activity is observed withthe starvation medium alone. This is compared to the output observedfrom the positive control samples (bFGF in growth medium) and proteindilutions.

Example 89 Detection of Inhibition of a Mixed Lymphocyte Reaction

This assay can be used to detect and evaluate inhibition of a MixedLymphocyte Reaction (MLR) by fusion proteins of the invention.Inhibition of a MLR may be due to a direct effect on cell proliferationand viability, modulation of costimulatory molecules on interactingcells, modulation of adhesiveness between lymphocytes and accessorycells, or modulation of cytokine production by accessory cells. Multiplecells may be targeted by the albumin fusion proteins that inhibit MLRsince the peripheral blood mononuclear fraction used in this assayincludes T, B and natural killer lymphocytes, as well as monocytes anddendritic cells.

Albumin fusion proteins of the invention found to inhibit the MLR mayfind application in diseases associated with lymphocyte and monocyteactivation or proliferation. These include, but are not limited to,diseases such as asthma, arthritis, diabetes, inflammatory skinconditions, psoriasis, eczema, systemic lupus erythematosus, multiplesclerosis, glomerulonephritis, inflammatory bowel disease, crohn'sdisease, ulcerative colitis, arteriosclerosis, cirrhosis, graft vs. hostdisease, host vs. graft disease, hepatitis, leukemia and lymphoma.

Briefly, PBMCs from human donors are purified by density gradientcentrifugation using Lymphocyte Separation Medium (LSM®, density 1.0770g/ml, Organon Teknika Corporation, West Chester, Pa.). PBMCs from twodonors are adjusted to 2×10⁶ cells/ml in RPMI-1640 (Life Technologies,Grand Island, N.Y.) supplemented with 10% FCS and 2 mM glutamine. PBMCsfrom a third donor is adjusted to 2×10⁵ cells/ml. Fifty microliters ofPBMCs from each donor is added to wells of a 96-well round bottommicrotiter plate. Dilutions of the fusion protein test material (50 μl)is added in triplicate to microtiter wells. Test samples (of the proteinof interest) are added for final dilution of 1:4; rhuIL-2 (R&D Systems,Minneapolis, Minn., catalog number 202-IL) is added to a finalconcentration of 1 μg/ml; anti-CD4 mAb (R&D Systems, clone 34930.11,catalog number MAB379) is added to a final concentration of 10 μg/ml.Cells are cultured for 7-8 days at 37° C. in 5% CO₂, and 1 μC of [³H]thymidine is added to wells for the last 16 hrs of culture. Cells areharvested and thymidine incorporation determined using a PackardTopCount. Data is expressed as the mean and standard deviation oftriplicate determinations.

Samples of the fusion protein of interest are screened in separateexperiments and compared to the negative control treatment, anti-CD4mAb, which inhibits proliferation of lymphocytes and the positivecontrol treatment, IL-2 (either as recombinant material or supernatant),which enhances proliferation of lymphocytes.

Example 90 Assays for Protease Activity

The following assay may be used to assess protease activity of analbumin fusion protein of the invention.

Gelatin and casein zymography are performed essentially as described(Heusen et al., Anal. Biochem., 102:196-202 (1980); Wilson et al.,Journal of Urology, 149:653-658 (1993)). Samples are run on 10%polyacryamide/0.1% SDS gels containing 1% gelain orcasein, soaked in2.5% triton at room temperature for 1 hour, and in 0.1M glycine, pH 8.3at 37° C. 5 to 16 hours. After staining in amido black areas ofproteolysis appear as clear areas against the blue-black background.Trypsin (Sigma T8642) is used as a positive control.

Protease activity is also determined by monitoring the cleavage ofn-a-benzoyl-L-arginine ethyl ester (BAEE) (Sigma B-4500. Reactions areset up in (25 mMNaPO₄,1 mM EDTA, and 1 mM BAEE), pH 7.5. Samples areadded and the change in adsorbance at 260 nm is monitored on the BeckmanDU-6 spectrophotometer in the time-drive mode. Trypsin is used as apositive control.

Additional assays based upon the release of acid-soluble peptides fromcasein or hemoglobin measured as adsorbance at 280 nm orcolorimetrically using the Folin method are performed as described inBergmeyer, et al., Methods of Enzymatic Analysis, 5 (1984). Other assaysinvolve the solubilization of chromogenic substrates (Ward, AppliedScience, 251-317 (1983)).

Example 91 Identifying Serine Protease Substrate Specificity

Methods known in the art or described herein may be used to determinethe substrate specificity of the albumin fusion proteins of the presentinvention having serine protease activity. A preferred method ofdetermining substrate specificity is by the use of positional scanningsynthetic combinatorial libraries as described in GB 2 324 529(incorporated herein in its entirety).

Example 92 Ligand Binding Assays

The following assay may be used to assess ligand binding activity of analbumin fusion protein of the invention.

Ligand binding assays provide a direct method for ascertaining receptorpharmacology and are adaptable to a high throughput format. The purifiedligand for an albumin fusion protein of the invention is radiolabeled tohigh specific activity (50-2000 Ci/mmol) for binding studies. Adetermination is then made that the process of radiolabeling does notdiminish the activity of the ligand towards the fusion protein. Assayconditions for buffers, ions, pH and other modulators such asnucleotides are optimized to establish a workable signal to noise ratiofor both membrane and whole cell polypeptide sources. For these assays,specific polypeptide binding is defined as total associatedradioactivity minus the radioactivity measured in the presence of anexcess of unlabeled competing ligand. Where possible, more than onecompeting ligand is used to define residual nonspecific binding.

Example 93 Functional Assay in Xenopus Oocytes

Capped RNA transcripts from linearized plasmid templates encoding analbumin fusion protein of the invention is synthesized in vitro with RNApolymerases in accordance with standard procedures. In vitro transcriptsare suspended in water at a final concentration of 0.2 mg/mi. Ovarianlobes are removed from adult female toads, Stage V defolliculatedoocytes are obtained, and RNA transcripts (10 ng/oocyte) are injected ina 50 nl bolus using a microinjection apparatus. Two electrode voltageclamps are used to measure the currents from individual Xenopus oocytesin response fusion protein and polypeptide agonist exposure. Recordingsare made in Ca2+ free Barth's medium at room temperature. The Xenopussystem can be used to screen known ligands and tissue/cell extracts foractivating ligands.

Example 94 Microphysiometric Assays

Activation of a wide variety of secondary messenger systems results inextrusion of small amounts of acid from a cell. The acid formed islargely as a result of the increased metabolic activity required to fuelthe intracellular signaling process. The pH changes in the mediasurrounding the cell are very small but are detectable by the CYTOSENSORmicrophysiometer (Molecular Devices Ltd., Menlo Park, Calif.). TheCYTOSENSOR is thus capable of detecting the ability of an albumin fusionprotein of the invention to activate secondary messengers that arecoupled to an energy utilizing intracellular signaling pathway.

Example 95 Extract/Cell Supernatant Screening

A large number of mammalian receptors exist for which there remains, asyet, no cognate activating ligand (agonist). Thus, active ligands forthese receptors may not be included within the ligands banks asidentified to date. Accordingly, the albumin fusion proteins of theinvention can also be functionally screened (using calcium, cAMP,microphysiometer, oocyte electrophysiology, etc., functional screens)against tissue extracts to identify natural ligands for the Therapeuticprotein portion and/or albumin protein portion of an albumin fusionprotein of the invention. Extracts that produce positive functionalresponses can be sequentially subfractionated until an activating ligandis isolated and identified.

Example 96 ATP-Binding Assay

The following assay may be used to assess ATP-binding activity of fusionproteins of the invention.

ATP-binding activity of an albumin fusion protein of the invention maybe detected using the ATP-binding assay described in U.S. Pat. No.5,858,719, which is herein incorporated by reference in its entirety.Briefly, ATP-binding to an albumin fusion protein of the invention ismeasured via photoaffinity labeling with 8-azido-ATP in a competitionassay. Reaction mixtures containing 1 mg/ml of ABC transport protein areincubated with varying concentrations of ATP, or the non-hydrolyzableATP analog adenyl-5′-imidodiphosphate for 10 minutes at 4° C. A mixtureof 8-azido-ATP (Sigma Chem. Corp., St. Louis, Mo.) plus 8-azido-ATP(³²P-ATP) (5 mCi/μmol, ICN, Irvine Calif.) is added to a finalconcentration of 100 μM and 0.5 ml aliquots are placed in the wells of aporcelain spot plate on ice. The plate is irradiated using a short wave254 nm UV lamp at a distance of 2.5 cm from the plate for two one-minuteintervals with a one-minute cooling interval in between. The reaction isstopped by addition of dithiothreitol to a final concentration of 2 mM.The incubations are subjected to SDS-PAGE electrophoresis, dried, andautoradiographed. Protein bands corresponding to the albumin fusionproteins of the invention are excised, and the radioactivity quantified.A decrease in radioactivity with increasing ATP oradenyl-5′-imidodiphosphate provides a measure of ATP affinity to thefusion protein.

Example 97 Phosphorylation Assay

In order to assay for phosphorylation activity of an albumin fusionprotein of the invention, a phosphorylation assay as described in U.S.Pat. No. 5,958,405 (which is herein incorporated by reference) isutilized. Briefly, phosphorylation activity may be measured byphosphorylation of a protein substrate using gamma-labeled ³²P-ATP andquantitation of the incorporated radioactivity using a gammaradioisotope counter. The fusion protein of the invention is incubatedwith the protein substrate, ³²P-ATP, and a kinase buffer. The ³²Pincorporated into the substrate is then separated from free ³²P-ATP byelectrophoresis, and the incorporated ³²P is counted and compared to anegative control. Radioactivity counts above the negative control areindicative of phosphorylation activity of the fusion protein.

Example 98 Detection of Phosphorylation Activity (Activation) of anAlbumin Fusion Protein of the Invention in the Presence of PolypeptideLigands

Methods known in the art or described herein may be used to determinethe phosphorylation activity of an albumin fusion protein of theinvention. A preferred method of determining phosphorylation activity isby the use of the tyrosine phosphorylation assay as described in U.S.Pat. No. 5,817,471 (incorporated herein by reference).

Example 99 Identification of Signal Transduction Proteins that Interactwith an Albumin Fusion Protein of the Present Invention

Albumin fusion proteins of the invention may serve as research tools forthe identification, characterization and purification of signaltransduction pathway proteins or receptor proteins. Briefly, a labeledfusion protein of the invention is useful as a reagent for thepurification of molecules with which it interacts. In one embodiment ofaffinity purification, an albumin fusion protein of the invention iscovalently coupled to a chromatography column. Cell-free extract derivedfrom putative target cells, such as carcinoma tissues, is passed overthe column, and molecules with appropriate affinity bind to the albuminfusion protein. The protein complex is recovered from the column,dissociated, and the recovered molecule subjected to N-terminal proteinsequencing. This amino acid sequence is then used to identify thecaptured molecule or to design degenerate oligonucleotide probes forcloning the relevant gene from an appropriate cDNA library.

Example 100 IL-6 Bioassay

A variety of assays are known in the art for testing the proliferativeeffects of an albumin fusion protein of the invention. For example, onesuch assay is the IL-6 Bioassay as described by Marz et al. (Proc. Natl.Acad. Sci., U.S.A., 95:3251-56 (1998), which is herein incorporated byreference). After 68 hrs. at 37° C., the number of viable cells ismeasured by adding the tetrazolium salt thiazolyl blue (MTT) andincubating for a further 4 hrs. at 37° C. B9 cells are lysed by SDS andoptical density is measured at 570 nm. Controls containing IL-6(positive) and no cytokine (negative) are Briefly, IL-6 dependent B9murine cells are washed three times in IL-6 free medium and plated at aconcentration of 5,000 cells per well in 50 μl, and 50 μl of fusionprotein of the invention is added. utilized. Enhanced proliferation inthe test sample(s) (containing an albumin fusion protein of theinvention) relative to the negative control is indicative ofproliferative effects mediated by the fusion protein.

Example 101 Support of Chicken Embryo Neuron Survival

To test whether sympathetic neuronal cell viability is supported by analbumin fusion protein of the invention, the chicken embryo neuronalsurvival assay of Senaldi et at may be utilized (Proc. Natl. Acad. Sci.,U.S.A., 96:11458-63 (1998), which is herein incorporated by reference).Briefly, motor and sympathetic neurons are isolated from chickenembryos, resuspended in L15 medium (with 10% FCS, glucose, sodiumselenite, progesterone, conalbumin, putrescine, and insulin; LifeTechnologies, Rockville, Md.) and Dulbecco's modified Eagles medium[with 10% FCS, glutamine, penicillin, and 25 mM Hepes buffer (pH 7.2);Life Technologies, Rockville, Md.], respectively, and incubated at 37°C. in 5% CO₂ in the presence of different concentrations of the purifiedfusion protein of the invention, as well as a negative control lackingany cytokine. After 3 days, neuron survival is determined by evaluationof cellular morphology, and through the use of the colorimetric assay ofMosmann (Mosmann, T., J. Immunol. Methods, 65:55-63 (1983)). Enhancedneuronal cell viability as compared to the controls lacking cytokine isindicative of the ability of the albumin fusion protein to enhance thesurvival of neuronal cells.

Example 102 Assay for Phosphatase Activity

The following assay may be used to assess serine/threonine phosphatase(PTPase) activity of an albumin fusion protein of the invention.

In order to assay for serine/threonine phosphatase (PTPase) activity,assays can be utilized which are widely known to those skilled in theart. For example, the serine/threonine phosphatase (PSPase) activity ofan albumin fusion protein of the invention may be measured using aPSPase assay kit from New England Biolabs, Inc. Myelin basic protein(MyBP), a substrate for PSPase, is phosphorylated on serine andthreonine residues with cAMP-dependent Protein Kinase in the presence of[³²P]ATP. Protein serine/threonine phosphatase activity is thendetermined by measuring the release of inorganic phosphate from32P-labeled MyBP.

Example 103 Interaction of Serine/Threonine Phosphatases with OtherProteins

Fusion protein of the invention having serine/threonine phosphataseactivity (e.g., as determined in Example 102) are useful, for example,as research tools for the identification, characterization andpurification of additional interacting proteins or receptor proteins, orother signal transduction pathway proteins. Briefly, a labeled fusionprotein of the invention is useful as a reagent for the purification ofmolecules with which it interacts. In one embodiment of affinitypurification, an albumin fusion protein of the invention is covalentlycoupled to a chromatography column. Cell-free extract derived fromputative target cells, such as neural or liver cells, is passed over thecolumn, and molecules with appropriate affinity bind to the fusionprotein. The fusion protein-complex is recovered from the column,dissociated, and the recovered molecule subjected to N-terminal proteinsequencing. This amino acid sequence is then used to identify thecaptured molecule or to design degenerate oligonucleotide probes forcloning the relevant gene from an appropriate cDNA library.

Example 104 Assaying for Heparanase Activity

There a numerous assays known in the art that may be employed to assayfor heparanase activity of an albumin fusion protein of the invention.In one example, heparanase activity of an albumin fusion protein of theinvention, is assayed as described by Vlodaysky et al., (Vlodaysky etal., Nat. Med., 5:793-802 (1999)). Briefly, cell lysates, conditionedmedia, intact cells (1×10⁶ cells per 35-mm dish), cell culturesupernatant, or purified fusion protein are incubated for 18 hrs at 37°C., pH 6.2-6.6, with ³⁵S-labeled ECM or soluble ECM derived peak Iproteoglycans. The incubation medium is centrifuged and the supernatantis analyzed by gel filtration on a Sepharose CL-6B column (0.9×30 cm).Fractions are eluted with PBS and their radioactivity is measured.Degradation fragments of heparan sulfate side chains are eluted fromSepharose 6B at 0.5<K_(av)<0.8 (peak II). Each experiment is done atleast three times. Degradation fragments corresponding to “peak II,” asdescribed by Vlodaysky et al., is indicative of the activity of analbumin fusion protein of the invention in cleaving heparan sulfate.

Example 105 Immobilization of Biomolecules

This example provides a method for the stabilization of an albuminfusion protein of the invention in non-host cell lipid bilayerconstructs (see, e.g., Bieri et al., Nature Biotech 17:1105-1108 (1999),hereby incorporated by reference in its entirety herein) which can beadapted for the study of fusion proteins of the invention in the variousfunctional assays described above. Briefly, carbohydrate-specificchemistry for biotinylation is used to confine a biotin tag to analbumin fusion protein of the invention, thus allowing uniformorientation upon immobilization. A 50 uM solution of an albumin fusionprotein of the invention in washed membranes is incubated with 20 mMNaIO4 and 1.5 mg/ml (4 mM) BACH or 2 mg/ml (7.5 mM) biotin-hydrazide for1 hr at room temperature (reaction volume, 150 ul). Then the sample isdialyzed (Pierce Slidealizer Cassett, 10 kDa cutoff; Pierce ChemicalCo., Rockford Ill.) at 4C first for 5 h, exchanging the buffer aftereach hour, and finally for 12 h against 500 ml buffer R (0.15 M NaCl, 1mM MgCl2, 10 mM sodium phosphate, pH7). Just before addition into acuvette, the sample is diluted 1:5 in buffer ROG50 (Buffer Rsupplemented with 50 mM octylglucoside).

Example 106 Assays for Metalloproteinase Activity

Metalloproteinases are peptide hydrolases which use metal ions, such asZn²⁺, as the catalytic mechanism. Metalloproteinase activity of analbumin fusion protein of the present invention can be assayed accordingto methods known in the art. The following exemplary methods areprovided:

Proteolysis of Alpha-2-Macroglobulin

To confirm protease activity, a purified fusion protein of the inventionis mixed with the substrate alpha-2-macroglobulin (0.2 unit/ml;Boehringer Mannheim, Germany) in 1× assay buffer (50 mM HEPES, pH 7.5,0.2 M NaCl, 10 mM CaCl₂, 25 μM ZnCl₂ and 0.05% Brij-35) and incubated at37° C. for 1-5 days. Trypsin is used as positive control. Negativecontrols contain only alpha-2-macroglobulin in assay buffer. The samplesare collected and boiled in SDS-PAGE sample buffer containing 5%2-mercaptoethanol for 5-min, then loaded onto 8% SDS-polyacrylamide gel.After electrophoresis the proteins are visualized by silver staining.Proteolysis is evident by the appearance of lower molecular weight bandsas compared to the negative control.

Inhibition of Alpha-2-Macroglobulin Proteolysis by Inhibitors ofMetalloproteinases

Known metalloproteinase inhibitors (metal chelators (EDTA, EGTA, ANDHgCl₂), peptide metalloproteinase inhibitors (TIMP-1 and TIMP-2), andcommercial small molecule MMP inhibitors) may also be used tocharacterize the proteolytic activity of an albumin fusion protein ofthe invention. Three synthetic MMP inhibitors that may be used are: MMPinhibitor I, [IC₅₀=1.0 μM against MMP-1 and MMP-8; IC₅₀=30 μM againstMMP-9; IC₅₀=150 μM against MMP-3]; MMP-3 (stromelysin-1) inhibitor I[IC₅₀=5 μM against MMP-3], and MMP-3 inhibitor II [K_(i)=130 nM againstMMP-3]; inhibitors available through Calbiochem, catalog #444250,444218, and 444225, respectively). Briefly, different concentrations ofthe small molecule MMP inhibitors are mixed with a purified fusionprotein of the invention (50 μg/ml) in 22.9 μl of 1×HEPES buffer (50 mMHEPES, pH 7.5, 0.2 M NaCl, 10 mM CaCl₂, 25 μM ZnCl₂ and 0.05% Brij-35)and incubated at room temperature (24° C.) for 2-hr, then 7.1 μl ofsubstrate alpha-2-macroglobulin (0.2 unit/ml) is added and incubated at37° C. for 20-hr. The reactions are stopped by adding 4x sample bufferand boiled immediately for 5 minutes. After SDS-PAGE, the protein bandsare visualized by silver stain.

Synthetic Fluorogenic Peptide Substrates Cleavage Assay

The substrate specificity for fusion proteins of the invention withdemonstrated metalloproteinase activity may be determined usingtechniques known in the art, such as using synthetic fluorogenic peptidesubstrates (purchased from BACHEM Bioscience Inc). Test substratesinclude, M-1985, M-2225, M-2105, M-2110, and M-2255. The first four areMMP substrates and the last one is a substrate of tumor necrosisfactor-α (TNF-α) converting enzyme (TACE). These substrates arepreferably prepared in 1:1 dimethyl sulfoxide (DMSO) and water. Thestock solutions are 50-500 Fluorescent assays are performed by using aPerkin Elmer LS 50B luminescence spectrometer equipped with a constanttemperature water bath. The excitation λ is 328 nm and the emission λ is393 nm. Briefly, the assay is carried out by incubating 176 μl 1×HEPESbuffer (0.2 M NaCl, 10 mM CaCl₂, 0.05% Brij-35 and 50 mM HEPES, pH 7.5)with 4 μl of substrate solution (50 μM) at 25° C. for 15 minutes, andthen adding 20 μl of a purified fusion protein of the invention into theassay cuvette. The final concentration of substrate is 1 Initialhydrolysis rates are monitored for 30-min.

Example 107 Identification and Cloning of VII and VL Domains

One method to identify and clone VH and VL domains from cell linesexpressing a particular antibody is to perform PCR with VH and VLspecific primers on cDNA made from the antibody expressing cell lines.Briefly, RNA is isolated from the cell lines and used as a template forRT-PCR designed to amplify the VH and VL domains of the antibodiesexpressed by the EBV cell lines. Cells may be lysed in the TRIzol®reagent (Life Technologies, Rockville. Md.) and extracted with one fifthvolume of chloroform. After addition of chloroform, the solution isallowed to incubate at room temperature for 10 minutes, and thecentrifuged at 14,000 rpm for 15 minutes at 4° C. in a tabletopcentrifuge. The supernatant is collected and RNA is precipitated usingan equal volume of isopropanol. Precipitated RNA is pelleted bycentrifuging at 14,000 rpm for 15 minutes at 4° C. in a tabletopcentrifuge. Following centrifugation, the supernatant is discarded andwashed with 75% ethanol. Following washing, the RNA is centrifuged againat 800 rpm for 5 minutes at 4° C. The supernatant is discarded and thepellet allowed to air dry. RNA is the dissolved in DEPC water and heatedto 60° C. for 10 minutes. Quantities of RNA can determined using opticaldensity measurements.

cDNA may be synthesized, according to methods well-known in the art,from 1.5-2.5 micrograms of RNA using reverse transciptase and randomhexamer primers. cDNA is then used as a template for PCR amplificationof VH and VL domains. Primers used to amplify VH and VL genes are shownin Table 7. Typically a PCR reaction makes use of a single 5′ primer anda single 3′ primer. Sometimes, when the amount of available RNA templateis limiting, or for greater efficiency, groups of 5′ and/or 3′ primersmay be used. For example, sometimes all five VH-5′ primers and all JH3′primers are used in a single PCR reaction. The PCR reaction is carriedout in a 50 microliter volume containing 1×PCR buffer, 2 mM of eachdNTP, 0.7 units of High Fidelity Taq polymerase, 5′ primer mix, 3′primer mix and 7.5 microliters of cDNA. The 5′ and 3′ primer mix of bothVH and VL can be made by pooling together 22 pmole and 28 pmole,respectively, of each of the individual primers. PCR conditions are: 96°C. for 5 minutes; followed by 25 cycles of 94° C. for 1 minute, 50° C.for 1 minute, and 72° C. for 1 minute; followed by an extension cycle of72° C. for 10 minutes. After the reaction is completed, sample tubes arestored 4° C.

TABLE 7 Primer Sequences Used to Amplify VH and VL domains. Primer nameSEQ ID NO Primer Sequence (5′-3′) VH Primers Hu VH1-5′ 1056CAGGTGCAGCTGGTGCAGTCTGG Hu VH2-5′ 1057 CAGGTCAACTTAAGGGAGTCTGG Hu VH3-5′1058 GAGGTGCAGCTGGTGGAGTCTGG Hu VH4-5′ 1059 CAGGTGCAGCTGCAGGAGTCGGG HuVH5-5′ 1060 GAGGTGCAGCTGTTGCAGTCTGC Hu VH6-5′ 1061CAGGTACAGCTGCAGCAGTCAGG Hu JH1,2-5′ 1062 TGAGGAGACGGTGACCAGGGTGCC HuJH3-5′ 1063 TGAAGAGACGGTGACCATTGTCCC Hu JH4,5-5′ 1064TGAGGAGACGGTGACCAGGGTTCC Hu JH6-5′ 1065 TGAGGAGACGGTGACCGTGGTCCC VLPrimers Hu Vkappa1-5′ 1066 GACATCCAGATGACCCAGTCTCC Hu Vkappa2a-5′ 1067GATGTTGTGATGACTCAGTCTCC Hu Vkappa2b-5′ 1068 GATATTGTGATGACTCAGTCTCC HuVkappa3-5′ 1069 GAAATTGTGTTGACGCAGTCTCC Hu Vkappa4-5′ 1070GACATCGTGATGACCCAGTCTCC Hu Vkappa5-5′ 1071 GAAACGACACTCACGCAGTCTCC HuVkappa6-5′ 1072 GAAATTGTGCTGACTCAGTCTCC Hu Vlambda1-5′ 1073CAGTCTGTGTTGACGCAGCCGCC Hu Vlambda2-5′ 1074 CAGTCTGCCCTGACTCAGCCTGC HuVlambda3-5′ 1075 TCCTATGTGCTGACTCAGCCACC Hu Vlambda3b-5′ 1076TCTTCTGAGCTGACTCAGGACCC Hu Vlambda4-5′ 1077 CACGTTATACTGACTCAACCGCC HuVlambda5-5′ 1078 CAGGCTGTGCTCACTCAGCCGTC Hu Vlambda6-5′ 1079AATTTTATGCTGACTCAGCCCCA Hu Jkappa1-3′ 1080 ACGTTTGATTTCCACCTTGGTCCC HuJkappa2-3′ 1081 ACGTTTGATCTCCAGCTTGGTCCC Hu Jkappa3-3′ 1082ACGTTTGATATCCACTTTGGTCCC Hu Jkappa4-3′ 1083 ACGTTTGATCTCCACCTTGGTCCC HuJkappa5-3′ 1084 ACGTTTAATCTCCAGTCGTGTCCC Hu Jlambda1-3′ 1085CAGTCTGTGTTGACGCAGCCGCC Hu Jlambda2-3′ 1086 CAGTCTGCCCTGACTCAGCCTGC HuJlambda3--3′ 1087 TCCTATGTGCTGACTCAGCCACC Hu Jlambda3b-3′ 1088TCTTCTGAGCTGACTCAGGACCC Hu Jlambda4-3′ 1089 CACGTTATACTGACTCAACCGCC HuJlambda5-3′ 1090 CAGGCTGTGCTCACTCAGCCGTC Hu Jlambda6-3′ 1091AATTTTATGCTGACTCAGCCCCAPCR samples are then electrophoresed on a 1.3% agarose gel. DNA bands ofthe expected sizes (˜506 base pairs for VH domains, and 344 base pairsfor VL domains) can be cut out of the gel and purified using methodswell known in the art. Purified PCR products can be ligated into a PCRcloning vector (TA vector from Invitrogen Inc., Carlsbad, Calif.).Individual cloned PCR products can be isolated after transfection of E.coli and blue/white color selection. Cloned PCR products may then besequenced using methods commonly known in the art.

The PCR bands containing the VH domain and the VL domains can also beused to create full-length Ig expression vectors. VH and VL domains canbe cloned into vectors containing the nucleotide sequences of a heavy(e.g., human IgG1 or human IgG4) or light chain (human kappa or humanlambda) constant regions such that a complete heavy or light chainmolecule could be expressed from these vectors when transfected into anappropriate host cell. Further, when cloned heavy and light chains areboth expressed in one cell line (from either one or two vectors), theycan assemble into a complete functional antibody molecule that issecreted into the cell culture medium. Methods using polynucleotidesencoding VH and VL antibody domain to generate expression vectors thatencode complete antibody molecules are well known within the art.

Example 108 Construct ID 2672, HSA-T20, Generation

Construct ID 2672 (SEQ ID NO:1186), pSAC35:HSA.T20, comprises DNAencoding a T20 albumin fusion protein which has full length HSA fused tothe amino-terminus of the HIV-1 inhibitory peptide T20, i.e., Y643-F678,in the yeast S. cerevisiae expression vector pSAC35. The T20 peptide isderived from the ectodomain of the HIV-1 transmembrane protein gp41 andis shown to have inhibitory activity on HIV-1 infection.

Cloning of T20 cDNA

The polynucleotide encoding T20 was PCR generated using four overlappingprimers T20-1, T20-2, T20-3, and T20-4, described below. The sequencewas codon optimized for expression in yeast S. cerevisiae. The PCRfragment was cut with Bsu36I/Asc I, and ligated into Bsu36I/Asc I cutpScNHSA. A Not I fragment was then subcloned into the pSAC35 plasmid.Construct ID #2672 encodes an albumin fusion protein containing fulllength HSA and the HIV-1 inhibitory peptide T20, i.e., Tyr-643 toPhe-678 (SEQ ID NO:1188).

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the HIV-1inhibitory peptide T20, T20-1 and T20-4, were synthesized:

T20-1: (SEQ ID NO: 1189) 5′-AAGCTGCCTTAGGCTTATACACTAGTTTGATTCATAGTTTG-3′T20-2: (SEQ ID NO: 1204)5′-TACACTAGTTTGATTCATAGTTTGATTGAAGAAAGTCAAAATCAACA AGAAAAGAATGAACAAG-3′T20-3: (SEQ ID NO: 1205)5′-AAACCAATTCCACAAACTAGCCCATTTATCCAATTCCAACAATTCTTGTTCATTCTTTTCTTGTTGAT-3′ T20-4: (SEQ ID NO: 1190) 5′-TTGGCGCGCCTTAAAACCAATTCCACAAACTAGCCCATTTATCC-3′

T20-1 incorporates the Bsu 36I cloning site (shown underlined) andnucleotides encoding the last four amino acid residues of the matureform of HSA (SEQ ID NO:1038), as well as 24 nucleotides (shown in bold)encoding the first 8 amino acid residues of the HIV-1 inhibitory peptideT20, i.e., Tyr-643 to Leu-650. In T20-4, the Asc I site is underlinedand the last 31 nucleotides (shown in bold) are the reverse complementof DNA encoding the last 10 amino acid residues of the HIV-1 inhibitorypeptide T20, Asp-669 to Phe-678. The T20-2 and T20-3 oligonucleotidesoverlap with each other and with T20-1 and T20-4, respectively, andencode the HIV-1 inhibitory peptide T20. The PCR product was purified(for example, using Wizard PCR Preps DNA Purification System (PromegaCorp)) and then digested with Bsu36I and AscI. After furtherpurification of the Bsu36I-AscI fragment by gel electrophoresis, theproduct was cloned into Bsu36I/AscI digested pScNHSA. After the sequencewas confirmed, the expression cassette encoding this T20 albumin fusionprotein was subcloned into pSAC35 as a Not I fragment. A Not I fragmentwas further subcloned into pSAC35 to give construct ID #2672.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected HSA sequence (see below).

T20 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the HIV-1 inhibitory peptide T20, i.e., Tyr-643 toPhe-678. In one embodiment of the invention, T20 albumin fusion proteinsof the invention further comprise a signal sequence which directs thenascent fusion polypeptide in the secretory pathways of the host usedfor expression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature T20 albuminfusion protein is secreted directly into the culture medium. T20 albuminfusion proteins of the invention may comprise heterologous signalsequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, T20 albumin fusion proteins of theinvention comprise the native HIV-1 transmembrane protein gp41 signalsequence. In further preferred embodiments, the T20 albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Expression and Purification of Construct ID 2672.

Expression in Yeast S. cerevisiae.

Construct 2672 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted T20 albumin fusion proteinexpressed from construct ID #2672 in yeast S. cerevisiae can be purifiedas described in Example 4. N-terminal sequencing of the albumin fusionprotein should result in the sequence DARKS (SEQ ID NO:2143) whichcorresponds to the amino terminus of the mature form of HSA.

The Activity of T20 can be Assayed Using an In Vitro Infectivity Assayand/or a Cell-Cell Fusion Inhibition Assay.

The in vitro infectivity and cell-cell fusion inhibition assays aredescribed in Wild et al., “Peptides corresponding to a predictivealpha-helical domain of human immunodeficiency virus type 1 gp41 arepotent inhibitors of virus infection”, Proc. Natl. Acad. Sci. USA, 91:9770-9774 (1994)).

Method

High-titered virus stocks may be prepared in CEM human leukemia cells asdescribed previously (see Wild, C., et al., “A synthetic peptideinhibitor of human immunodeficiency virus replication: correlationbetween solution structure and viral inhibition”, Proc. Natl. Acad. Sci.USA 89: 10537-10541 (1992)). Infectious titers may be estimated byend-point dilution on AA5 and CEM continuous cell-lines. Reversetranscriptase (RT) activity present in the supernatants may be taken ascriteria for successful infection. The 50% tissue culture infection dose(TCID₅₀) may be calculated by using the formula of Reed and Muench (seeWild et al., “Peptides corresponding to a predictive alpha-helicaldomain of human immunodeficiency virus type 1 gp41 are potent inhibitorsof virus infection”, Proc. Natl. Acad. Sci. USA, 91: 9770-9774 (1994)).Primary HIV-1 isolates may be expanded in activated peripheral bloodmononuclear cells, “PBMC”, from normal donors.

The ability of the T20 albumin fusion protein to inhibit infection withprototypic cell-free virus, i.e., HIV-1_(LAI) or HIV-1_(NIHZ), may beevaluated by incubating serial dilutions of cell-free virus with AA5 orCEM target cells containing various concentrations of the T20 albuminfusion protein. The T20 albumin fusion protein may be tested againstprimary isolates and the prototypic HIV-1_(LAI) isolate in a similarassay using PBMC as target cells. Both assays are carried out asdescribed in Wild et al., 1992.

The ability of the T20 albumin fusion protein to block virus-mediatedcell-cell fusion may be assessed as described previously in Wild et al.,1992. Briefly, approximately 7×10⁴ MOLT-4 cells may be incubated with10⁴ CEM cells and chronically infected with the HIV-1 isolates in96-well plates (half-area cluster plates; Costar) in 100 μL of culturemedium. The T20 albumin fusion protein may be added in 10 μL and thecell mixtures may be incubated for 24 hrs at 37° C. At that time,multinucleated giant cells may be estimated by microscopic examinationat ×40 magnification.

The Activity of T20 Albumin Fusion Encoded by Construct ID #2672 can beAssayed Using an In Vitro Infectivity Assay and/or a Cell-Cell FusionInhibition Assay.

Method

The T20 albumin fusion protein encoded by construct 2672 can be testedin the in vitro infectivity bioassay as well as the cell-cell fusioninhibition assay as described above under subsection heading, “Theactivity of T20 can be assayed using an in vitro Infectivity Assayand/or a Cell-Cell Fusion Inhibition Assay”.

Example 109 Construct ID 2673, T20-HSA, Generation

Construct ID 2673, pSAC35:T20.HSA, comprises DNA encoding a T20 albuminfusion protein which has the HSA chimeric leader sequence, i.e., theHSA-kex2 signal peptide, followed by the HIV-1 inhibitory peptide T20,i.e., Y643-F678, fused to the amino-terminus of the mature form of HSAin the yeast S. cerevisiae expression vector pSAC35.

Cloning of T20 cDNA

The DNA encoding the HIV-1 inhibitory peptide was PCR generated usingfour overlapping primers. The sequence was codon optimized forexpression in yeast S. cerevisiae. The PCR fragment was digested withSal I/Cla I and subcloned into Xho I/Cla I digested pScCHSA. A Not Ifragment was then subcloned into the pSAC35 plasmid. Construct ID #2673encodes for the chimeric leader sequence of HSA fused to the HIV-1inhibitory peptide T20, i.e., Tyr-643 to Phe-678, followed by the matureform of HSA.

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the HIV-1inhibitory peptide T20, T20-5 and T20-6, were synthesized:

T20-5: (SEQ ID NO: 1192)5′-AGGAGCGTCGACAAAAGATACACTAGTTTGATTCATAGTTTG-3′ T20-6: (SEQ ID NO:1193) 5′-CGCGCATCGATGAGCAACCTCACTCTTGTGTGCATCAAACCAATTCCACAAACTAGCCCATTTATCC-3′T20-5 incorporates a Sal I cloning site (shown underlined), nucleotidesencoding the last three amino acid residues of the HSA chimeric leadersequence, and the DNA encoding the first 8 amino acids (shown in bold)of the HIV-1 inhibitory peptide T20, i.e., Tyr-643 to Leu-650. In T20-6,the underlined sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein (SEQ ID NO:1038). The boldedsequence is the reverse complement of the 31 nucleotides encoding thelast 10 amino acid residues Asp-669 to Phe-678 of the HIV-1 inhibitorypeptide T20. The T20-2 and T20-3 oligonucleotides (as in Example 108)overlap with each other and with T20-5 and T20-6, respectively, andencode the HIV-1 inhibitory peptide T20. Using these primers, the HIV-1inhibitory peptide T20 was generated by annealing, extension of theannealed primers, digestion with Sal I and Cla I, and subcloning intoXho I/Cla I digested pScCHSA. After the sequence was confirmed, the NotI fragment containing the T20 albumin fusion expression cassette wassubcloned into pSAC35 cut with Not I to generate construct ID 2673.Construct ID #2673 encodes an albumin fusion protein containing thechimeric leader sequence, the HIV-1 inhibitory peptide T20, and themature form of HSA.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected T20 sequence (see below).

T20 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the HIV-1 inhibitory peptide T20, i.e., Tyr-643 toPhe-678. In one embodiment of the invention, T20 albumin fusion proteinsof the invention further comprise a signal sequence which directs thenascent fusion polypeptide in the secretory pathways of the host usedfor expression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature T20 albuminfusion protein is secreted directly into the culture medium. T20 albuminfusion proteins of the invention may comprise heterologous signalsequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, T20 albumin fusion proteins of theinvention comprise the native HIV-1 transmembrane protein gp41 signalsequence. In further preferred embodiments, the T20 albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Expression and Purification of Construct ID 2673.

Expression in Yeast S. cerevisiae.

Construct 2673 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted T20 albumin fusion proteinexpressed from construct ID #2673 in yeast S. cerevisiae can be purifiedas described in Example 4. N-terminal sequencing of the expressed andpurified albumin fusion protein should generate YTSLI (SEQ ID NO:2151)which corresponds to the amino terminus of the HIV-1 inhibitory peptideT20.

The Activity of T20 Albumin Fusion Encoded by Construct ID #2673 can beAssayed Using an In Vitro Infectivity Assay and/or a Cell-Cell FusionInhibition Assay.

Method

The T20 albumin fusion protein encoded by construct 2673 can be testedin the in vitro infectivity bioassay as well as the cell-cell fusioninhibition assay as described above in Example 108 under subsectionheading, “The activity of T20 can be assayed using an in vitroInfectivity Assay and/or a Cell-Cell Fusion Inhibition Assay”.

Example 110 Indications for T20 Albumin Fusion Proteins

Based on the activity of T20 albumin fusion proteins in the aboveassays, T20 albumin fusion proteins are useful in treating, preventing,and/or diagnosing HIV, AIDS, and/or SIV (simian immunodeficiency virus)infections.

Example 111 Construct ID 2667, HSA-T1249, Generation

Construct ID 2667, pSAC35:HSA.T1249, comprises DNA encoding a T1249albumin fusion protein which has the full length HSA protein, includingthe native HSA leader sequence, fused to the amino-terminus of thesecond-generation fusion inhibitor peptide, “T1249”, i.e., W1-F39, inthe yeast S. cerevisiae expression vector pSAC35. The T1249 peptide is asecond-generation fusion inhibitor derived from the HIV-1 transmembraneprotein gp41 and is shown to have inhibitory activity on HIV-1infection.

Cloning of T1249 cDNA

The polynucleotide encoding T1249 was PCR generated using fouroverlapping primers T1249-1, T1249-2, T1249-3, and T1249-4, describedbelow. The sequence was codon optimized for expression in yeast S.cerevisiae. The PCR fragment was cut with Bsu 36I/Asc I, and ligatedinto Bsu 36I/Asc I cut pScNHSA. A Not I fragment was then subcloned intothe pSAC35 plasmid. Construct ID #2667 encodes an albumin fusion proteincontaining the full length HSA protein, including the native HSA leadersequence, fused to the T1249 peptide, i.e., Trp-1 to Phe-39.

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the T1249 peptide,T1249-1 and T1249-4, were synthesized:

T1249-1: (SEQ ID NO: 1181) 5′-AAGCTGCCTTAGGCTTATGGCAAGAATGGGAACAAAAG-3′T1249-2: (SEQ ID NO: 1206)5′-TGGCAAGAATGGGAACAAAAGATTACTGCTTTGTTAGAACAAGCTCAAATTCAACAAGAAAAGAATGAAT-3′ T1249-3: (SEQ ID NO: 1207)5′-GAACCATTCCCATAAAGAAGCCCATTTATCCAACTTTTGCAATTCATATTCATTCTTTTCTTGTTGAATTTGAGCTT-3′ T1249-4: (SEQ ID NO: 1182)5′-TTGGCGCGCC TTAGAACCATTCCCATAAAGAAGCCCATTTATC-3′

T1249-1 incorporates the Bsu 36I cloning site (shown underlined) andnucleotides encoding the last four amino acid residues of the matureform of HSA (SEQ ID NO:1038), as well as 21 nucleotides (shown in bold)encoding the first 7 amino acid residues of the T1249 peptide, i.e.,Trp-1 to Lys-7. In T1249-4, the Asc I site is underlined and the last 30nucleotides (shown in bold) are the reverse complement of DNA encodingthe last 10 amino acid residues of the T1249 peptide, Asp-30 to Phe-39.The T1249-2 and T1249-3 oligonucleotides overlap with each other andwith T1249-1 and T1249-4, respectively, and encode the T1249 peptide.The PCR product was purified (for example, using Wizard PCR Preps DNAPurification System (Promega Corp)) and then digested with Bsu36I andAscI. After further purification of the Bsu36I-AscI fragment by gelelectrophoresis, the product was cloned into Bsu36I/AscI digestedpScNHSA. After the sequence was confirmed, the expression cassetteencoding this T1249 albumin fusion protein was subcloned into pSAC35 asa Not I fragment. A Not I fragment was further subcloned into pSAC35 togive construct ID #2667.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected HSA sequence (see below).

T1249 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the HIV-1 inhibitory peptide T1249, i.e., Trp-1 to Phe-39.In one embodiment of the invention, T1249 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature T1249 albuminfusion protein is secreted directly into the culture medium. T1249albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, T1249 albumin fusion proteins of theinvention comprise the native HIV-1 transmembrane protein gp41 signalsequence. In further preferred embodiments, the T1249 albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

Expression and Purification of Construct ID 2667.

Expression in Yeast S. cerevisiae.

Construct 2667 can be transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3). Expression levels can be examined byimmunoblot detection with anti-HSA serum as the primary antibody.

Purification from Yeast S. cerevisiae Cell Supernatant.

The cell supernatant containing the secreted T1249 albumin fusionprotein expressed from construct ID #2667 in yeast S. cerevisiae can bepurified as described in Example 4. N-terminal sequencing of the albuminfusion protein should result in the sequence DARKS which corresponds tothe amino terminus of the mature form of HSA.

The Activity of T1249 Albumin Fusion Encoded by Construct ID #2667 canbe Assayed Using an In Vitro Infectivity Assay and/or a Cell-Cell FusionInhibition Assay.

Method

The T1249 albumin fusion protein encoded by construct 2667 can be testedin the in vitro infectivity bioassay as well as the cell-cell fusioninhibition assay as described above in Example 108 under subsectionheading, “The activity of T20 can be assayed using an in vitroInfectivity Assay and/or a Cell-Cell Fusion Inhibition Assay”.

Example 112 Construct ID 2670, T1249-HSA, Generation

Construct ID 2670, pSAC35:T1249.HSA, comprises DNA encoding a T1249albumin fusion protein which has the HSA chimeric leader sequence, i.e.,the HSA-kex2 signal peptide, the second-generation fusion inhibitorpeptide, “T1249”, i.e., W1-F39 fused to the amino-terminus of the matureform of HSA in the yeast S. cerevisiae expression vector pSAC35.

Cloning of T1249 cDNA

The DNA encoding the second-generation fusion inhibitor peptide was PCRgenerated using four overlapping primers. The sequence was codonoptimized for expression in yeast S. cerevisiae. The PCR fragment wasdigested with Sal I/Cla I and subcloned into Xho I/Cla I digestedpScCHSA. A Not I fragment was then subcloned into the pSAC35 plasmid.Construct ID #2670 encodes for the chimeric leader sequence of HSA fusedto the T1249 peptide, i.e., Trp-1 to Phe-39, followed by the mature formof HSA.

The 5′ and 3′ primers of the four overlapping oligonucleotides suitablefor PCR amplification of the polynucleotide encoding the T1249 peptide,T1249-5 and T1249-6, were synthesized:

T1249-5: (SEQ ID NO: 1184) 5′-AGGAGCGTCGACAAAAGATGGCAAGAATGGGAACAAAAG-3′T1249-6: (SEQ ID NO: 1185)5′-ATCGATGAGCAACCTCACTCTTGTGTGCATCGAACCATTCCCATAAA GAAGCCCATTTATC-3′

T1249-5 incorporates a Sal I cloning site (shown underlined),nucleotides encoding the last three amino acid residues of the HSAchimeric leader sequence, and the DNA encoding the first 7 amino acids(shown in bold) of the T1249 peptide, i.e., Trp-1 to Lys-7. In T1249-6,the underlined sequence is a Cla I site; and the Cla I site and the DNAfollowing it are the reverse complement of DNA encoding the first 10amino acids of the mature HSA protein (SEQ ID NO:1038). The boldedsequence is the reverse complement of the 30 nucleotides encoding thelast 10 amino acid residues Asp-30 to Phe-39 of the T1249 peptide. TheT1249-2 and T1249-3 oligonucleotides (as in Example 111) overlap witheach other and with T1249-5 and T1249-6, respectively, and encode theT1249 peptide. Using these primers, the T1249 peptide was generated byannealing, extension of the annealed primers, digestion with Sal I andCla I, and subcloning into Xho I/Cla I digested pScCHSA. After thesequence was confirmed, the Not I fragment containing the T1249 albuminfusion expression cassette was subcloned into pSAC35 cut with Not I togenerate construct ID 2670. Construct ID #2670 encodes an albumin fusionprotein containing the chimeric leader sequence, the T1249 peptide, andthe mature form of HSA.

Further, analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected T1249 sequence (see below).

T1249 albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the T1249 peptide, i.e., Trp-1 to Phe-39. In oneembodiment of the invention, T1249 albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature T1249 albuminfusion protein is secreted directly into the culture medium. T1249albumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MAF, INV, Ig, Fibulin B,Clusterin, Insulin-Like Growth Factor Binding Protein 4, variant HSAleader sequences including, but not limited to, a chimeric HSA/MAFleader sequence, or other heterologous signal sequences known in theart. In a preferred embodiment, T1249 albumin fusion proteins of theinvention comprise the native HIV-1 transmembrane protein gp41 signalsequence. In further preferred embodiments, the T1249 albumin fusionproteins of the invention further comprise an N-terminal methionineresidue. Polynucleotides encoding these polypeptides, includingfragments and/or variants, are also encompassed by the invention.

The Activity of T1249 Albumin Fusion Encoded by Construct ID #2670 canbe Assayed Using an In Vitro Infectivity Assay and/or a Cell-Cell FusionInhibition Assay.

Method

The T1249 albumin fusion protein encoded by construct 2670 can be testedin the in vitro infectivity bioassay as well as the cell-cell fusioninhibition assay as described above in Example 108 under subsectionheading, “The activity of T20 can be assayed using an in vitroInfectivity Assay and/or a Cell-Cell Fusion Inhibition Assay”.

Example 113 Indications for T1249 Albumin Fusion Proteins

Based on the activity of T1249 albumin fusion proteins in the aboveassays, T1249 albumin fusion proteins are useful in treating,preventing, and/or diagnosing HIV, AIDS, and/or SIV (simianimmunodeficiency virus) infections.

Example 114 Construct ID 2702, HSA-GCSF.T31-L201, Generation

Construct ID 2702, pSAC35:HSA.GCSF.T31-L201, comprises DNA encoding aGCSF albumin fusion protein which has mature HSA fused downstream of theHSA/kex2 leader sequence and upstream of amino acids T31 to L201 ofGCSF, in the yeast S. cerevisiae expression vector pSAC35.

Cloning of GCSF cDNA

The polynucleotide encoding the GCSF C-terminal deletion mutant was PCRamplified using primers GCSF-5 and GCSF-6, described below. The amplimerwas cut with Bsu36I and AscI, and ligated into pScNHSA. Construct ID#2702 encodes an albumin fusion protein containing mature HSA fuseddownstream of the HSA/kex2 leader sequence and upstream of amino acidsT31 to L201 of GCSF.

Two oligonucleotide primers, GCSF-5 and GCSF-6, suitable for PCRamplification of the polynucleotide encoding the GCSF C-terminaldeletion mutant, were synthesized:

GCSF-5: (SEQ ID NO: 1197) 5′-AAGCTGCCTTAGGCTTAACCCCCCTGGGCCCTGCCAGGCSF-6: (SEQ ID NO: 1198) 5′-GCGCGCGGCGCGCCTCAAAGGTGGCGTAGAACGCGGTACGAC

GCSF-5 incorporates the Bsu36I cloning site (shown underlined), andnucleotides encoding the last six amino acids of HSA as well as thefirst six amino acids of mature GCSF (amino acids T31 through A36).GCSF-6 contains an AscI cloning site (shown underlined) and the last 25nucleotides are the reverse complement of DNA encoding the last eightamino acid residues of the GCSF C-terminal deletion mutant (S194 throughL201). The PCR product generated with these primers was purified (forexample, using Wizard PCR Preps DNA Purification System (PromegaCorporation)) and then digested with Bsu36I and AscI. After furtherpurification of the Bsu36I/AscI PCR fragment by gel electrophoresis, theproduct was cloned into Bsu36I/AscI digested pScNHSA. After the sequencewas confirmed, the expression cassette encoding this GCSF albumin fusionprotein was subcloned into pSAC35 as a NotI fragment.

Further analysis of the N-terminus of the expressed albumin fusionprotein by amino acid sequencing can confirm the presence of theexpected HSA sequence (see below).

GCSF albumin fusion proteins of the invention preferably comprise themature form of HSA, i.e., Asp-25 to Leu-609, fused to either the N- orC-terminus of the C-terminal deletion mutant of GCSF, i.e., T31 to L201.In one embodiment of the invention, GCSF albumin fusion proteins of theinvention further comprise a signal sequence which directs the nascentfusion polypeptide in the secretory pathways of the host used forexpression. In a further preferred embodiment, the signal peptideencoded by the signal sequence is removed, and the mature GCSF albuminfusion protein is secreted directly into the culture medium. GCSFalbumin fusion proteins of the invention may comprise heterologoussignal sequences including, but not limited to, MFα-1, Invertase, Ig,Fibulin B, Clusterin, Insulin-like growth factor binding protein 4, K.lactis killer toxin, and variant HSA leader sequences including, but notlimited to, a chimeric HSA/MFα-1 (HSA/kex2) leader sequence, a chimericK. lactis/MFα-1 leader sequence, or other heterologous signal sequencesknown in the art. In a further preferred embodiment, GCSF albumin fusionproteins of the invention comprise the native GCSF signal sequence. Infurther preferred embodiments, the GCSF albumin fusion proteins of theinvention further comprise and N-terminal methionine residue.Polynucleotides encoding these polypeptides, including fragments and/orvariants are also encompassed by the invention.

Expression and Purification of Construct ID #2702

Expression in Yeast S. cerevisiae

Construct #2702 was transformed into yeast S. cerevisiae by methodsknown in the art (see Example 3) and as previously described forconstruct ID #1642 (see Example 19). Expression levels were examined byimmunoblot detection with anti-HSA serum as the primary antibody (datanot shown).

Purification from Yeast S. cerevisiae Cell Supernatant

A general procedure for purification of albumin fusion proteins isdescribed in Example 4. The cell supernatant containing GCSF albuminfusion protein expressed from construct ID #2702 in yeast S. cerevisiaewas purified as described in Example 20. N-terminal sequencing of thealbumin fusion protein should result in the sequence DARKS whichcorresponds to the amino terminus of the mature form of HSA.

The Activity of GCSF Albumin Fusion Encoded by Construct ID #2702 can beAssayed Using an In Vitro NFS-60 Cell Proliferation Assay. Method

The GCSF albumin fusion protein encoded by construct 2702 was testedusing the in vitro NFS-60 cell proliferation bioassay previouslydescribed in Example 19 under subsection headings “The activity of GCSFcan be assayed using an in vitro NFS-60 cell proliferation assay” and“The activity of GCSF albumin fusion encoded by construct ID #1642 canbe assayed using an in vitro NFS-60 cell proliferation assay”.

Results

Both the partially purified GCSF albumin fusion protein encoded byconstruct 1634 (HSA-GCSF) and the GCSF C-terminal deletion mutantalbumin fusion protein (L-171) encoded by construct 2702 demonstratedthe ability to cause NFS-60 cell proliferation, with the C-terminaldeletion mutant exhibiting a more potent proliferative effect (see FIG.19). Unexpectedly, the fusion protein encoded by construct 2702exhibited 2-3 times more activity than the fusion protein encoded byconstruct 1643. Alternate GCSF albumin fusion constructs comprisealbumin fused to amino acid residues 1-169 of mature GCSF and albuminfused to amino acid residues 1-170 of mature GCSF.

Example 115 Construct ID 2876, HSA-IFNα Hybrid

Construct ID 2876, pSAC35:HSA.IFNαA(C1-Q91)/D(L93-E166) R23K,A113Vcomprises DNA encoding an IFNα hybrid albumin fusion protein which hasmature HSA fused downstream of the HSA/kex2 leader sequence and upstreamof an IFNα A/D hybrid amino acid sequence, in the yeast S. cerevisiaeexpression vector pSAC35. Regarding the composition of the hybrid IFN,the first 91 amino acids are from the subtype IFNα2 (also called IFNαA)and the remaining 75 aa are from IFNα1 (IFNαD). We incorporated twopoint mutations (R23K, A113V). The fusion was generated by PCR and fuseddownstream of HSA within the yeast expression vector pSAC35.

Results CID 2876 Expression and Purification

The yeast strain BXP-10 was transformed with pSAC35:CID 2876 and atransformant selected for fermentation. A 5-liter fermentation wasperformed and analysis of supernatant demonstrated high expression(approximately 500 mg/l). A small proportion of the supernatant wasprocessed to pilot purification. Approximately 1 mg of CID 2876 protein(greater than 95% pure based on N-terminal sequence) was obtainedfollowing a purification through Blue-sepharose, followed by gelfiltration, followed by Q-anion exchange. The remaining fermentationstarting material is available for further purification if needed.

ISRE Activity

All type I IFNs mediate their activities through engagement of a commonIFN receptor complex and activation of the ISRE signal transductionpathway. Activation of gene transcription through this pathway leads tothe cellular responses associated with IFNs includinganti-proliferation, antiviral and immune modulation. Using a reporterbased strategy, the ability of CID 2876 to activate the ISRE signaltransduction pathway was determined. CID 2876 was found to be a potentactivator of the ISRE pathway, demonstrating an EC₅₀ of 2.7 ng/ml (datanot shown). This compares favorably with the potency of CID 3165 in thisassay system.

Anti-Viral Activity

A hallmark activity of IFNs is their ability to mediate cellularprotection against viral infection. While most human type I IFNs displayantiviral activity in a species restricted manner, the hybrid IFNemployed in this study has been demonstrated to be active on murinecells. Thus the antiviral activity of CID 2876 was evaluated on themurine cell line L929 infected with EMCV. Results indicate that CID 2876does demonstrate antiviral activity in a cross species manner (data notshown).

Example 116 Activity of Construct 3070 (GLP-1 Albumin Fusion) Measuredby In Vitro Stimulation of Insulin mRNA in INS-1 Cells

It has recently been shown that GLP-1 increases the expression ofinsulin mRNA in pancreatic beta-cells (Buteau et al., Diabetologia 1999July; 42(7):856-64). Thus, the ability of the GLP-1 albumin fusionprotein encoded by CID 3070 to stimulate insulin mRNA was evaluatedusing the pancreatic beta-cell line INS-1 (832/13).

FIG. 14 illustrates the steady-state levels of insulin mRNA in INS-1(832/13) cells after treatment with GLP-1 or GLP-1 albumin fusionprotein encoded by construct ID 3070 (CID 3070 protein). Both GLP-1 andthe CID 3070 protein stimulate transcription of the insulin gene. Thefirst bar (black) represents the untreated cells. Bars 2-4 (white)represent cells treated with the indicated concentrations of GLP-1. Bars5-7 (gray) represent cells treated with the indicated concentrations ofCID 3070 protein.

It will be clear that the invention may be practiced otherwise than asparticularly described in the foregoing description and examples.Numerous modifications and variations of the present invention arepossible in light of the above teachings and, therefore, are within thescope of the appended claims.

The entire disclosure of each document cited (including patents, patentapplications, patent publications, journal articles, abstracts,laboratory manuals, books, or other disclosures) as well as informationavailable through Identifiers specific to databases such as GenBank,GeneSeq, or the CAS Registry, referred to in this application are hereinincorporated by reference in their entirety.

Furthermore, the specification and sequence listing of each of thefollowing U.S. applications are herein incorporated by reference intheir entirety: U.S. Application No. 60/341,811, filed Dec. 21, 2001;U.S. Application No. 60/360,000, filed Feb. 28, 2002; U.S. ApplicationNo. 60/378,950, filed May 10, 2002; U.S. Application No. 60/398,008,filed Jul. 24, 2002; U.S. Application No. 60/411,355, filed Sep. 18,2002; U.S. Application No. 60/414,984, filed Oct. 2, 2002; U.S.Application No. 60/417,611, filed Oct. 11, 2002; U.S. Application No.60/420,246, filed Oct. 23, 2002; U.S. Application No. 60/423,623, filedNov. 5, 2002; U.S. Application No. 60/350,358, filed Jan. 24, 2002; U.S.Application No. 60/359,370, filed Feb. 26, 2002; U.S. Application No.60/367,500, filed Mar. 27, 2002; U.S. Application No. 60/402,131, filedAug. 9, 2002; U.S. Application No. 60/402,708, filed Aug. 13, 2002; U.S.Application No. 60/351,360, filed Jan. 28, 2002; U.S. Application No.60/382,617, filed May 24, 2002; U.S. Application No. 60/383,123, filedMay 28, 2002; U.S. Application No. 60/385,708, filed Jun. 5, 2002; U.S.Application No. 60/394,625, filed Jul. 10, 2002; U.S. Application No.60/411,426, filed Sep. 18, 2002; U.S. Application No. 60/370,227, filedApr. 8, 2002; U.S. Application No. 60/351,360 filed Jan. 28, 2002; U.S.Application No. 60/382,617, filed May 24, 2002; U.S. Application No.60/383,123, filed May 28, 2002; U.S. Application No. 60/385,708, filedJun. 5, 2002; U.S. Application No. 60/394,625, filed Jul. 10, 2002; andU.S. Application No. 60/411,426, filed Sep. 18, 2002. Furthermore, thespecification and sequence listing of U.S. application, Human GenomeSciences, Inc. attorney docket number PF574PCT, filed concurrentlyherewith on Dec. 23, 2002, is hereby incorporated by reference in itsentirety.

What is claimed:
 1. An albumin fusion protein comprising a memberselected from the group consisting of: (a) a Therapeutic protein:X andalbumin comprising the amino acid sequence of SEQ ID NO:1038; (b) aTherapeutic protein:X and a fragment or a variant of the amino acidsequence of SEQ ID NO:1038, wherein said fragment or variant has albuminactivity; (c) a Therapeutic protein:X and a fragment or a variant of theamino acid sequence of SEQ ID NO:1038, wherein said fragment or varianthas albumin activity, and further wherein said albumin activity is theability to prolong the shelf life of the Therapeutic protein:X comparedto the shelf-life of the Therapeutic protein:X in an unfused state; (d)a Therapeutic protein:X and a fragment or a variant of the amino acidsequence of SEQ ID NO:1038, wherein said fragment or variant has albuminactivity, and further wherein the fragment or variant comprises theamino acid sequence of amino acids 1-387 of SEQ ID NO:1038; (e) afragment or variant of a Therapeutic protein:X and albumin comprisingthe amino acid sequence of SEQ ID NO:1038, wherein said fragment orvariant has a biological activity of the Therapeutic protein:X; (f) aTherapeutic protein:X, or fragment or variant thereof, and albumin, orfragment or variant thereof, of (a) to (e), wherein the Therapeuticprotein:X, or fragment or variant thereof, is fused to the N-terminus ofalbumin, or the N-terminus of the fragment or variant of albumin; (g) aTherapeutic protein:X, or fragment or variant thereof, and albumin, orfragment or variant thereof, of (a) to (e), wherein the Therapeuticprotein:X, or fragment or variant thereof, is fused to the C-terminus ofalbumin, or the C-terminus of the fragment or variant of albumin; (h) aTherapeutic protein:X, or fragment or variant thereof, and albumin, orfragment or variant thereof, of (a) to (e), wherein the Therapeuticprotein:X, or fragment or variant thereof, is fused to the N-terminusand C-terminus of albumin, or the N-terminus and the C-terminus of thefragment or variant of albumin; (i) a Therapeutic protein:X, or fragmentor variant thereof, and albumin, or fragment or variant thereof, of (a)to (e), which comprises a first Therapeutic protein:X, or fragment orvariant thereof, and a second Therapeutic protein:X, or fragment orvariant thereof, wherein said first Therapeutic protein:X, or fragmentor variant thereof, is different from said second Therapeutic protein:X,or fragment or variant thereof; (j) a Therapeutic protein:X, or fragmentor variant thereof, and albumin, or fragment or variant thereof, of (a)to (i), wherein the Therapeutic protein:X, or fragment or variantthereof, is separated from the albumin or the fragment or variant ofalbumin by a linker; and (k) a Therapeutic protein:X, or fragment orvariant thereof, and albumin, or fragment or variant thereof, of (a) to(j), wherein the albumin fusion protein has the following formula:R1-L-R2; R2-L-R1; or R1-L-R2-L-R1, and further wherein R1 is Therapeuticprotein:X, or fragment or variant thereof, L is a peptide linker, and R2is albumin comprising the amino acid sequence of SEQ ID NO:1038 or afragment or variant of albumin.
 2. The albumin fusion protein of claim1, wherein the in vitro biological activity of the Therapeuticprotein:X, or fragment or variant thereof, fused to albumin, or fragmentor variant thereof, is greater than the in vitro biological activity ofthe Therapeutic protein:X, or fragment or variant thereof, in an unfusedstate.
 3. The albumin fusion protein of claim 1, wherein the in vivobiological activity of the Therapeutic protein:X, or fragment or variantthereof, fused to albumin, or fragment or variant thereof, is greaterthan the in vivo biological activity of the Therapeutic protein:X, orfragment or variant thereof, in an unfused state.
 4. An albumin fusionprotein comprising a Therapeutic protein:X, or fragment or variantthereof, inserted into an albumin, or fragment or variant thereof,comprising the amino acid sequence of SEQ ID NO:1038 or fragment orvariant thereof.
 5. An albumin fusion protein comprising a Therapeuticprotein:X, or fragment or variant thereof, inserted into an albumin, orfragment or variant thereof, comprising an amino acid sequence selectedfrom the group consisting of: (a) amino acids 54 to 61 of SEQ IDNO:1038; (b) amino acids 76 to 89 of SEQ ID NO:1038; (c) amino acids 92to 100 of SEQ ID NO:1038; (d) amino acids 170 to 176 of SEQ ID NO:1038;(e) amino acids 247 to 252 of SEQ ID NO:1038; (f) amino acids 266 to 277of SEQ ID NO:1038; (g) amino acids 280 to 288 of SEQ ID NO:1038; (h)amino acids 362 to 368 of SEQ ID NO:1038; (i) amino acids 439 to 447 ofSEQ ID NO:1038; (j) amino acids 462 to 475 of SEQ ID NO:1038; (k) aminoacids 478 to 486 of SEQ ID NO:1038; and (l) amino acids 560 to 566 ofSEQ ID NO:1038.
 6. The albumin fusion protein of claim 1, which isnon-glycosylated.
 7. The albumin fusion protein of claim 4, which isnon-glycosylated.
 8. The albumin fusion protein of claim 1, which isexpressed in yeast.
 9. The albumin fusion protein of claim 8, whereinthe yeast is glycosylation deficient.
 10. The albumin fusion protein ofclaim 1, which is expressed by a mammalian cell.
 11. The albumin fusionprotein of claim 1, wherein the albumin fusion protein further comprisesa secretion leader sequence.
 12. A composition comprising the albuminfusion protein of claim 1 and a pharmaceutically acceptable carrier. 13.A kit comprising the composition of claim
 12. 14. A method of treating adisease or disorder in a patient, comprising the step of administeringthe albumin fusion protein of claim
 1. 15. The method of claim 14,wherein the disease or disorder comprises indication:Y.
 16. A method oftreating a patient with a disease or disorder that is modulated byTherapeutic protein:X, or fragment or variant thereof, comprising thestep of administering an effective amount of the albumin fusion proteinof claim
 1. 17. The method of claim 16, wherein the disease or disorderis indication:Y.
 18. A nucleic acid molecule comprising a polynucleotidesequence encoding the albumin fusion protein of claim
 1. 19. A vectorcomprising the nucleic acid molecule of claim
 18. 20. A host cellcomprising the nucleic acid molecule of claim 18.